https://not-yet-needed.pages.dev/atom.xml Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data. 2026-08-29T14:16:38.364Z Not Yet Needed https://not-yet-needed.pages.dev/recalls/H-1230-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1228-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1229-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0769-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0772-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0773-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2873-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1219-2026 2026-08-12T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1206-2026 2026-08-12T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1192-2026 2026-08-12T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1213-2026 2026-08-12T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1222-2026 2026-08-12T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1205-2026 2026-08-12T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1224-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0759-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0755-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0747-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0748-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0768-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0753-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0749-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0752-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/D-0766-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2914-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2945-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2919-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2912-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2943-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2926-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2948-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2928-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2930-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2925-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Z-2924-2026 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/Food-99453-20260819 2026-08-19T00:00:00.000Z

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

https://not-yet-needed.pages.dev/recalls/H-1225-2026 2026-08-19T00:00:00.000Z

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