Aug 3, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near...
Firm: Shoolin Pharma Chem LLP
Reason: CGMP Deviations:Noted during FDA inspection
openFDA source record
Jul 31, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Drugs
Class I
Ongoing
Reported Aug 19, 2026
Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufactured by: Liebe...
Firm: Liebel-Flarsheim Company LLC
Reason: Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
openFDA source record
Jul 30, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Drugs
Class II
Ongoing
Reported Aug 19, 2026
CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-60...
Firm: Heritage Pharmaceuticals Inc
Reason: Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
openFDA source record
Jul 29, 2026
7 loaded recalls began on this date. 0 Class I. 7 ongoing.
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Colum...
Firm: Apollo Care, LLC
Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
openFDA source record
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170...
Firm: Apollo Care, LLC
Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
openFDA source record
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 711...
Firm: Apollo Care, LLC
Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
openFDA source record
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Colum...
Firm: Apollo Care, LLC
Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
openFDA source record
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 711...
Firm: Apollo Care, LLC
Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
openFDA source record
Drugs
Class II
Ongoing
Reported Aug 19, 2026
SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170...
Firm: Apollo Care, LLC
Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
openFDA source record
Drugs
Class II
Ongoing
Reported Aug 19, 2026
CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Co...
Firm: Prestige Brands Holdings
Reason: Lack of assurance of sterility. The recall is due to potential contamination
openFDA source record
Jul 28, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Food
Class III
Ongoing
Reported Aug 19, 2026
Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE. MANUFACTURED FOR: HONEYVILLE, INC. RANCHO CUCAMONGA, CA 917...
Firm: FlavorsandColor.Com
Reason: Undeclared Red #40.
openFDA source record
Jul 23, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Food
Class II
Ongoing
Reported Aug 19, 2026
Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.
Firm: SHEANDRO LLC
Reason: Label declares cream and cheese, but Milk is not declared
openFDA source record
Jul 22, 2026
2 loaded recalls began on this date. 2 Class I. 2 ongoing.
Food
Class I
Ongoing
Reported Aug 19, 2026
Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-60902 1. Distributed by...
Firm: MIDWEST POULTRY SERVC C/O H & LELECTRIC
Reason: Possible Salmonella Enteritidis
openFDA source record
Food
Class I
Ongoing
Reported Aug 19, 2026
Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Truth, Natural Cage Free Grain Fed, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g,...
Firm: MIDWEST POULTRY SERVC C/O H & LELECTRIC
Reason: Possible Salmonella Enteritidis
openFDA source record
Jul 19, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Food
Class I
Ongoing
Reported Aug 12, 2026
Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administ...
Firm: FACTORY6, INC.
Reason: Possible Salmonella in Moringa Leaf Powder product.
openFDA source record
Jul 18, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Food
Class I
Ongoing
Reported Aug 12, 2026
Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2 oz (232g) UPC 1 00001 00029 7 and Sprig & Sprout Spi...
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.
openFDA source record
Jul 17, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Food
Not Yet Classified
Ongoing
Reported Aug 19, 2026
MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.
Firm: Taylor Farms de Mexico S. de R.L. de C.V.
Reason: Potential Cyclospora contamination.
openFDA source record
Jul 14, 2026
3 loaded recalls began on this date. 0 Class I. 3 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4) KIT, SINUS...
Firm: Cardinal Health 200, LLC
Reason: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
openFDA source record
Devices
Class II
Ongoing
Reported Aug 19, 2026
Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC
Firm: Cardinal Health 200, LLC
Reason: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
openFDA source record
Devices
Class II
Ongoing
Reported Aug 19, 2026
Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Catalog N...
Firm: Cardinal Health 200, LLC
Reason: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
openFDA source record
Jul 6, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Devices
Class I
Ongoing
Reported Aug 19, 2026
Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flush for IV...
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 matt...
openFDA source record
Jul 1, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Drugs
Class I
Ongoing
Reported Aug 19, 2026
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for inj...
Firm: Victory Medical Center Pharmacy
Reason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
openFDA source record
Jun 30, 2026
3 loaded recalls began on this date. 0 Class I. 3 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
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...
openFDA source record
Devices
Class II
Ongoing
Reported Aug 19, 2026
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
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...
openFDA source record
Devices
Class II
Ongoing
Reported Aug 19, 2026
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
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...
openFDA source record
Jun 29, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
Firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Reason: Firmware issue potentially leading to loss of geometry movements.
openFDA source record
Jun 24, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE BOX01482V2...
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 utiliza...
openFDA source record
Jun 15, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into t...
Firm: Terumo Medical Corporation
Reason: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
openFDA source record
Jun 4, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Food
Class I
Ongoing
Reported Aug 12, 2026
Selectos Latinos Requeson Mexicano Mexican Cottage Cheese, Net Weight 16 oz, packed into retail-sized clear plastic containers. Keep refrigerated.
Firm: La Colonia Foods Llc
Reason: Products may be contaminated with Listeria monocytogenes.
openFDA source record
Jun 1, 2026
3 loaded recalls began on this date. 3 Class I. 3 ongoing.
Food
Class I
Ongoing
Reported Aug 12, 2026
Clover Hill Dairy LLP, mild cheese variety (Snack Pack Assorted Regular Mild Stix White Colby, Marble Jack, Yummy Cheddar). Sold in approximate 0.40-lb (6.4oz) units. Unk...
Firm: Clover Hill Dairy, LLC
Reason: Product contaminated with Listeria monocytogenes.
openFDA source record
Food
Class I
Ongoing
Reported Aug 12, 2026
Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Jalapeno Cheddar, Pepper Jack, Sizzlin Colby with Habanero Peppers). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb,...
Firm: Clover Hill Dairy, LLC
Reason: Product contaminated with Listeria monocytogenes.
openFDA source record
Food
Class I
Ongoing
Reported Aug 12, 2026
Clover Hill Dairy LLP, Mild Cheese Variety (Yummy Cheddar, White Cheddar, White Colby, Monterey Jack, Marble Jack). Sold in 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. U...
Firm: Clover Hill Dairy, LLC
Reason: Product contaminated with Listeria monocytogenes.
openFDA source record
May 23, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Food
Class I
Ongoing
Reported Aug 19, 2026
Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.
Firm: Bazzini LLC
Reason: Undeclared peanuts
openFDA source record
May 22, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1010. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common bile duct w...
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).
openFDA source record
Apr 30, 2026
1 loaded recalls began on this date. 0 Class I. 1 ongoing.
Devices
Class II
Ongoing
Reported Aug 19, 2026
BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular ca...
Firm: MICROVENTION INC.
Reason: Due to an increase rate of balloon pinhole defects.
openFDA source record
Mar 21, 2026
1 loaded recalls began on this date. 1 Class I. 1 ongoing.
Drugs
Class I
Ongoing
Reported Aug 19, 2026
Kian Pee Wan Capsules, 30-count bottles
Firm: Buy-Herbal
Reason: Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
openFDA source record