BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Not Yet Needed//Recall Radar//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Recall Radar latest recalls
X-WR-CALDESC:Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data.
BEGIN:VEVENT
UID:H-1230-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Food recall: Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger\, M...
DESCRIPTION:Class I Ongoing Firm: MIDWEST POULTRY SERVC C/O H & LELECTRIC Reason: Possible Salmonella Enteritidis Distribution: Arkansas\, Louisiana\, Mississippi\, New Mexico\, Oklahoma\, Texas Recall began: 2026-07-22 FDA IDs: H-1230-2026 / event 99479 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1230-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1230-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1228-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Food recall: Dark Chocolate Coconut Almond Bites\, 3.17oz\, Plastic Pouches\, 10 Packages per case.
DESCRIPTION:Class I Ongoing Firm: Bazzini LLC Reason: Undeclared peanuts Distribution: The product was distributed to WA. Recall began: 2026-05-23 FDA IDs: H-1228-2026 / event 99097 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1228-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1228-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1229-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Food recall: Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Tr...
DESCRIPTION:Class I Ongoing Firm: MIDWEST POULTRY SERVC C/O H & LELECTRIC Reason: Possible Salmonella Enteritidis Distribution: Arkansas\, Louisiana\, Mississippi\, New Mexico\, Oklahoma\, Texas Recall began: 2026-07-22 FDA IDs: H-1229-2026 / event 99479 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1229-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1229-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0769-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: Kian Pee Wan Capsules\, 30-count bottles
DESCRIPTION:Class I Ongoing Firm: Buy-Herbal Reason: Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. Distribution: Product was sold to individual consumers via ebay third party seller. Recall began: 2026-03-21 FDA IDs: D-0769-2026 / event 98650 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0769-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0769-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0772-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: Glutathione (MDV)\, 200 mg/mL\, 30 mL vial\, each mL contains Glutathione 200 mg\, Ascorbic Ac...
DESCRIPTION:Class I Ongoing Firm: Victory Medical Center Pharmacy Reason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. Distribution: USA Nationwide Recall began: 2026-07-01 FDA IDs: D-0772-2026 / event 99509 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0772-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0772-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0773-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: Optiray Imaging Bulk Package-350\, Ioversol Injection 74%\, 350 mg/mL Organically Bound Iodi...
DESCRIPTION:Class I Ongoing Firm: Liebel-Flarsheim Company LLC Reason: Presence of Particulate Matter: comprising polyethylene and other plastic materials\, stainless steel and glass. Distribution: Distributed Nationwide in the US and Mexico. Recall began: 2026-07-31 FDA IDs: D-0773-2026 / event 99510 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0773-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0773-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2873-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection\, 0.9%...
DESCRIPTION:Class I Ongoing Firm: Spectra Medical Devices\, Llc Reason: Manufacturing firm\, Huons\, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised\, patients may be exposed to microorganisms\, endotoxins\, or foreign matter. This may trigger inflammatory responses\, infec... Distribution: Distributed in the United States to medical device kit packers in six (6) states - CA\, FL\, NC\, OK\, TX\, VA. Recall began: 2026-07-06 FDA IDs: Z-2873-2026 / event 98777 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2873-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2873-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1219-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260812
DTEND;VALUE=DATE:20260813
SUMMARY:Food recall: Selectos Latinos Requeson Mexicano Mexican Cottage Cheese\, Net Weight 16 oz\, packed into r...
DESCRIPTION:Class I Ongoing Firm: La Colonia Foods Llc Reason: Products may be contaminated with Listeria monocytogenes. Distribution: The recalled product was distributed to the following states: MD\, VA Recall began: 2026-06-04 FDA IDs: H-1219-2026 / event 99325 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1219-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1219-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1206-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260812
DTEND;VALUE=DATE:20260813
SUMMARY:Food recall: Clover Hill Dairy LLP\, mild cheese variety (Snack Pack Assorted Regular Mild Stix White Co...
DESCRIPTION:Class I Ongoing Firm: Clover Hill Dairy\, LLC Reason: Product contaminated with Listeria monocytogenes. Distribution: MD\, VA\, NY Recall began: 2026-06-01 FDA IDs: H-1206-2026 / event 99211 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1206-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1206-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1192-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260812
DTEND;VALUE=DATE:20260813
SUMMARY:Food recall: Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Br...
DESCRIPTION:Class I Ongoing Firm: M.G. Foods\, Inc. Reason: Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label. Distribution: Product was shipped to the following states: AL\, GA\, KY\, NC\, SC\, TN\, VA & WV. Recall began: 2026-07-18 FDA IDs: H-1192-2026 / event 99458 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1192-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1192-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1213-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260812
DTEND;VALUE=DATE:20260813
SUMMARY:Food recall: Clover Hill Dairy LLP\, Pepper Jack Cheese Varieties (Jalapeno Cheddar\, Pepper Jack\, Sizzli...
DESCRIPTION:Class I Ongoing Firm: Clover Hill Dairy\, LLC Reason: Product contaminated with Listeria monocytogenes. Distribution: MD\, VA\, NY Recall began: 2026-06-01 FDA IDs: H-1213-2026 / event 99211 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1213-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1213-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1222-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260812
DTEND;VALUE=DATE:20260813
SUMMARY:Food recall: Zen Principle Naturals Moringa Leaf Powder dietary supplement\, 900mg capsules\, 180 capsule...
DESCRIPTION:Class I Ongoing Firm: FACTORY6\, INC. Reason: Possible Salmonella in Moringa Leaf Powder product. Distribution: Distributed to Nevada for further distribution. Recall began: 2026-07-19 FDA IDs: H-1222-2026 / event 99425 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1222-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1222-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1205-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260812
DTEND;VALUE=DATE:20260813
SUMMARY:Food recall: Clover Hill Dairy LLP\, Mild Cheese Variety (Yummy Cheddar\, White Cheddar\, White Colby\, Mon...
DESCRIPTION:Class I Ongoing Firm: Clover Hill Dairy\, LLC Reason: Product contaminated with Listeria monocytogenes. Distribution: MD\, VA\, NY Recall began: 2026-06-01 FDA IDs: H-1205-2026 / event 99211 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1205-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1205-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1224-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Food recall: Vodka Tomato Sauce\, NET WT. 24 oz / 680g\, glass jar packed 12 jars in a carton.
DESCRIPTION:Class II Ongoing Firm: SHEANDRO LLC Reason: Label declares cream and cheese\, but Milk is not declared Distribution: Product distributed in Florida Recall began: 2026-07-23 FDA IDs: H-1224-2026 / event 99516 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1224-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1224-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0759-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SILDENAFIL CITRATE USP\, 0.100 KG\, 100 gm-bag Net Wt\, RX ONLY "FOR Prescription Compounding...
DESCRIPTION:Class II Ongoing Firm: Shoolin Pharma Chem LLP Reason: CGMP Deviations:Noted during FDA inspection Distribution: Distributed Nationwide in the USA Recall began: 2026-08-03 FDA IDs: D-0759-2026 / event 99547 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0759-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0759-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0755-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SEMAGLUTIDE 7.5mg (5mg/mL)\, Glycine 7.5 mg (5mg/mL)\, 1.5 mL Sterile Multi-Dose Vial\, Rx On...
DESCRIPTION:Class II Ongoing Firm: Apollo Care\, LLC Reason: Presence of Particulate Matter\; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution: Nationwide within the U.S Recall began: 2026-07-29 FDA IDs: D-0755-2026 / event 99505 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0755-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0755-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0747-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SEMAGLUTIDE 12.5MG (2.5MG/mL)\, 5 mL Sterile Multi-Dose Vial\, Rx Only\, For Subcutaneous Inj...
DESCRIPTION:Class II Ongoing Firm: Apollo Care\, LLC Reason: Presence of Particulate Matter\; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution: Nationwide within the U.S Recall began: 2026-07-29 FDA IDs: D-0747-2026 / event 99505 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0747-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0747-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0748-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SEMAGLUTIDE 2.25MG (0.9 mg/mL)\, 2.5 mL Sterile Multi-Dose Vial\, Rx Only\, For Subcutaneous...
DESCRIPTION:Class II Ongoing Firm: Apollo Care\, LLC Reason: Presence of Particulate Matter\; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution: Nationwide within the U.S Recall began: 2026-07-29 FDA IDs: D-0748-2026 / event 99505 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0748-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0748-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0768-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION\, USP\, 75 mg/5 mL\, Rx Only\, 100 mL\, D...
DESCRIPTION:Class II Ongoing Firm: Heritage Pharmaceuticals Inc Reason: Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles. Distribution: Nationwide within the U.S Recall began: 2026-07-30 FDA IDs: D-0768-2026 / event 99526 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0768-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0768-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0753-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SEMAGLUTIDE 2.5mg (1mg/mL)\, Glycine 12.5 mg (5mg/mL)\, 2.5 mL Sterile Multi-Dose Vial\, Rx O...
DESCRIPTION:Class II Ongoing Firm: Apollo Care\, LLC Reason: Presence of Particulate Matter\; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution: Nationwide within the U.S Recall began: 2026-07-29 FDA IDs: D-0753-2026 / event 99505 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0753-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0753-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0749-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SEMAGLUTIDE 6.75mg (4.5 mg/mL)\, 1.5 mL Sterile Multi-Dose Vial\, Rx Only\, For Subcutaneous...
DESCRIPTION:Class II Ongoing Firm: Apollo Care\, LLC Reason: Presence of Particulate Matter\; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution: Nationwide within the U.S Recall began: 2026-07-29 FDA IDs: D-0749-2026 / event 99505 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0749-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0749-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0752-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: SEMAGLUTIDE 0.9mg (0.9 mg/mL)\, 1 mL Sterile Multi-Dose Vial\, Rx Only\, For Subcutaneous Inj...
DESCRIPTION:Class II Ongoing Firm: Apollo Care\, LLC Reason: Presence of Particulate Matter\; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution: Nationwide within the U.S Recall began: 2026-07-29 FDA IDs: D-0752-2026 / event 99505 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0752-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0752-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0766-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Drugs recall: CLEAR EYES Maximum Itchy Eye Relief\, 0.5 fl oz (15 mL) per dropper bottle\, Sterile\, Dist....
DESCRIPTION:Class II Ongoing Firm: Prestige Brands Holdings Reason: Lack of assurance of sterility. The recall is due to potential contamination Distribution: Nationwide in the USA. Recall began: 2026-07-29 FDA IDs: D-0766-2026 / event 99532 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0766-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0766-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2914-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: GORE VIABIL Short Wire Biliary Endoprosthesis\, Model No. VSWVN1010. Flexible\, self-expandi...
DESCRIPTION:Class II Ongoing Firm: W L Gore & Associates\, Inc. Reason: 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010). Distribution: U.S. Nationwide distribution in the states of GA and RI. Recall began: 2026-05-22 FDA IDs: Z-2914-2026 / event 99143 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2914-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2914-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2945-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Cardinal Health Presource Kits: 1) ENT TRAY \, Catalog Number: 24-0726A\; 2) KIT\,SINUS \, Cat...
DESCRIPTION:Class II Ongoing Firm: Cardinal Health 200\, LLC Reason: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. Distribution: US Nationwide. Canada. Recall began: 2026-07-14 FDA IDs: Z-2945-2026 / event 99380 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2945-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2945-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2919-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY P...
DESCRIPTION:Class II Ongoing Firm: Covidien\, LP Reason: Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures\, which may lead to infection\, loss of vision if in ophthalmic utilization\, or prolonged surgery. Distribution: US Nationwide and the countries of Australia\, Austria\, Belgium\, Bulgaria\, Canada\, Canary Islands\, Chile\, China\, Colombia\, Croatia\, Cyprus\, Czech Republic\, Denmark\, Estonia\, Finland\, France\, Germany\, Greece\, Guadeloupe\, Guatemala\, Honduras\, Hong Kong\, Hungary\,... Recall began: 2026-06-24 FDA IDs: Z-2919-2026 / event 99390 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2919-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2919-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2912-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BG...
DESCRIPTION:Class II Ongoing Firm: MICROVENTION INC. Reason: Due to an increase rate of balloon pinhole defects. Distribution: Worldwide - U.S. Nationwide distribution in the states of AL\, AR\, AZ\, CA\, FL\, GA\, IA\, IL\, KS\, KY\, LA\, MI\, MN\, MO\, MT\, NC\, NH\, NM\, NY\, OH\, PA\, SD\, TN\, TX\, WA\, and WI. The countries of Europe - Austria\, Belgium\, Denmark\, Finland\, France\, Germany\, Greece\, Iceland... Recall began: 2026-04-30 FDA IDs: Z-2912-2026 / event 98909 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2912-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2912-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2943-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK \, Catalog Number: SOP30SP...
DESCRIPTION:Class II Ongoing Firm: Cardinal Health 200\, LLC Reason: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. Distribution: US Nationwide. Canada. Recall began: 2026-07-14 FDA IDs: Z-2943-2026 / event 99380 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2943-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2943-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2926-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes\, 12" x 12"\, 110 Count Bag\, Product Numbe...
DESCRIPTION:Class II Ongoing Firm: Medline Industries\, LP Reason: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced bleach concentration may compromise the effectiveness of disinfection\,... Distribution: US Nationwide distribution in the states and territories of Guam\, Puerto Rico. Recall began: 2026-06-30 FDA IDs: Z-2926-2026 / event 99432 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2926-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2926-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2948-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Cardinal Health Presource Kits: 1) KIT\, MER NEURO BACK \, Catalog Number: PN33NBMYD\; 2) KIT...
DESCRIPTION:Class II Ongoing Firm: Cardinal Health 200\, LLC Reason: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels. Distribution: US Nationwide. Canada. Recall began: 2026-07-14 FDA IDs: Z-2948-2026 / event 99380 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2948-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2948-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2928-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Allura Xper FD. Model Numbers: 722026\, 722027\, 722028\, 722029\, 722035\, 722038\, 722039\, 722...
DESCRIPTION:Class II Ongoing Firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Reason: Firmware issue potentially leading to loss of geometry movements. Distribution: Worldwide distribution - US Nationwide and the countries of Canada\, Algeria\, Argentina\, Australia\, Austria\, Bangladesh\, Belarus\, Belgium\, Brazil\, Bulgaria\, Chile\, China\, Colombia\, Costa Rica\, Croatia\, Cuba\, Czech Republic\, Denmark\, Ecuador\, Egypt\, Finland\, Fra... Recall began: 2026-06-29 FDA IDs: Z-2928-2026 / event 99378 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2928-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2928-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2930-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glid...
DESCRIPTION:Class II Ongoing Firm: Terumo Medical Corporation Reason: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. Distribution: Worldwide distribution - US Nationwide and the country of Canada. Recall began: 2026-06-15 FDA IDs: Z-2930-2026 / event 99285 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2930-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2930-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2925-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes\, 12" x 12"\, 110 Count\, Product Number MS...
DESCRIPTION:Class II Ongoing Firm: Medline Industries\, LP Reason: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced bleach concentration may compromise the effectiveness of disinfection\,... Distribution: US Nationwide distribution in the states and territories of Guam\, Puerto Rico. Recall began: 2026-06-30 FDA IDs: Z-2925-2026 / event 99432 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2925-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2925-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-2924-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Devices recall: Medline Micro-Kill Bleach Germicidal Bleach Wipes\, 6" x 5"\, 150 count\, Product Number MSC3...
DESCRIPTION:Class II Ongoing Firm: Medline Industries\, LP Reason: Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced bleach concentration may compromise the effectiveness of disinfection\,... Distribution: US Nationwide distribution in the states and territories of Guam\, Puerto Rico. Recall began: 2026-06-30 FDA IDs: Z-2924-2026 / event 99432 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2924-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2924-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Food-99453-20260819@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Food recall: MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg\, Romaine\, Carrots\, Red Cabbage p...
DESCRIPTION:Not Yet Classified Ongoing Firm: Taylor Farms de Mexico S. de R.L. de C.V. Reason: Potential Cyclospora contamination. Distribution: Domestic: AL\, AR\, CT\, FL\, GA\, IA\, IL\, IN\, KS\, KY\, LA\, MA\, MD\, MI\, MO\, MS\, NC\, NH\, NJ\, OH\, OK\, PA\, SC\, TN\, TX\, VA\, and WI Foreign: Mexico. Recall began: 2026-07-17 FDA IDs: / event 99453 Source: https://api.fda.gov/food/enforcement.json?search=event_id%3A%2299453%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=event_id%3A%2299453%22
END:VEVENT
BEGIN:VEVENT
UID:H-1225-2026@not-yet-needed.pages.dev
DTSTAMP:20260829T201533Z
DTSTART;VALUE=DATE:20260819
DTEND;VALUE=DATE:20260820
SUMMARY:Food recall: Honeyville YELLOW COLOR 1 GALLON NFI: WATER\, FD&C YELLOW #5\, FD&C YELLOW #6\, CITRIC ACID\,...
DESCRIPTION:Class III Ongoing Firm: FlavorsandColor.Com Reason: Undeclared Red #40. Distribution: Product is sold to independent manufacturer locations in Nevada\, Arizona\, Oregon\, and California.12 locations total. Recall began: 2026-07-28 FDA IDs: H-1225-2026 / event 99540 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1225-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1225-2026%22
END:VEVENT
END:VCALENDAR