FDA recalls
8 recalls published in the last 7 days. Food, medicines, medical devices, meat and poultry, consumer products and vehicles – 547 recalls since Aug 17, 2026, each with the lot codes, dates and model numbers exactly as the agency lists them.
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Latest recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 | Potential cracks in the hose, which could lead to leakage or the hose falling off. Most serious | FDA Class I | |
| Oct 7, 2026 | a fire hazard Most serious | FDA Class I | |
| Oct 7, 2026 | possible Salmonella contamination Most serious | FDA Class I | |
| Oct 7, 2026 | possible Salmonella contamination Most serious | FDA Class I | |
| Oct 7, 2026 | possible Salmonella and E. coli contamination Most serious | FDA Class I | |
| Oct 7, 2026 | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II | |
| Oct 7, 2026 | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II | |
| Oct 7, 2026 | The potential for falsely elevated results. Serious | FDA Class II | |
| Oct 7, 2026 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II | |
| Oct 7, 2026 | Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may outpu… Serious | FDA Class II | |
| Oct 7, 2026 | While in the high-power operating mode, a video dropout/blackout may occur when using a pa… Serious | FDA Class II | |
| Oct 7, 2026 | Screws, intended for use with polyaxial compression plating system intended for foot osteo… Serious | FDA Class II | |
| Oct 7, 2026 | Potential for monomer liquid leakage. Serious | FDA Class II | |
| Oct 7, 2026 | Breast biopsy and tissue removal system may experience the following errors: 1) Probe cali… Serious | FDA Class II | |
| Oct 7, 2026 | a labeling error Serious | FDA Class II | |
| Oct 7, 2026 | There are identified discrepancies between the sterilization parameters listed in the Inst… Serious | FDA Class II | |
| Oct 7, 2026 | Retrospectively reported correction for an instrument intended for targeted sequencing of … Serious | FDA Class II | |
| Oct 7, 2026 | hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may… Serious | FDA Class II | |
| Oct 7, 2026 | an increased risk of a crash Serious | FDA Class II | |
| Oct 7, 2026 | Due to manufacturing issues reperfusion catheters may fracture. Serious | FDA Class II | |
| Oct 7, 2026 | Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gl… Serious | FDA Class II | |
| Oct 7, 2026 | Due to manufacturing issues with the liquid skin adhesive containing in surgical convenien… Serious | FDA Class II | |
| Oct 7, 2026 | Software system may associate image data from one patient with another patient's record, p… Serious | FDA Class II | |
| Oct 7, 2026 | Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter … Serious | FDA Class II | |
| Oct 7, 2026 | a fall hazard Serious | FDA Class II | |
| Oct 7, 2026 | Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunc… Serious | FDA Class II | |
| Oct 7, 2026 | Positron emission tomography and computed tomography x-ray systems have a software problem… Serious | FDA Class II | |
| Oct 7, 2026 | Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformatio… Serious | FDA Class II | |
| Oct 7, 2026 | Due to blood-to-glycol leak in the heat exchanger. Serious | FDA Class II | |
| Oct 7, 2026 | When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR… Serious | FDA Class II | |
| Oct 7, 2026 | Due to incorrect expiration date on product manufactured between September 2016 to March 2… Serious | FDA Class II | |
| Oct 7, 2026 | Failed Dissolution Specifications: below specification Serious | FDA Class II | |
| Oct 7, 2026 | Crystallization Serious | FDA Class II | |
| Oct 7, 2026 | Failed dissolution specifications. Serious | FDA Class II | |
| Oct 7, 2026 | Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient ou… Serious | FDA Class II | |
| Oct 7, 2026 | a sterility problem Serious | FDA Class II | |
| Oct 7, 2026 | Defective Container; packets were found to be either empty or partially full. Serious | FDA Class II | |
| Oct 7, 2026 | microbial contamination Serious | FDA Class II | |
| Oct 7, 2026 | undeclared shellfish Serious | FDA Class II | |
| Oct 7, 2026 | undeclared allergen ingredient Serious | FDA Class II | |
| Oct 7, 2026 | undeclared yellow Serious | FDA Class II | |
| Oct 7, 2026 | undeclared sugar Serious | FDA Class II | |
| Oct 7, 2026 | Product contains garlic essential oil not approved for culinary use Serious | FDA Class II | |
| Oct 7, 2026 | lead Serious | FDA Class II | |
| Oct 7, 2026 | Products were distributed without the required Maintenance Supplement, which describes an … Lower risk | FDA Class III | |
| Sep 30, 2026 | Tip may fracture or detach, leading to device fragments remaining within the patient or mi… Most serious | FDA Class I | |
| Sep 30, 2026 | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminat… Most serious | FDA Class I | |
| Sep 30, 2026 | Potential to exhibit a loose connection between the flexible tubing and the nasal cannula,… Most serious | FDA Class I | |
| Sep 30, 2026 | possible Salmonella contamination Most serious | FDA Class I | |
| Sep 30, 2026 | possible Listeria contamination Most serious | FDA Class I |
Recalls by brand
How to read a recall
Identifiers decide whether your product is included. A recall almost never covers every package with a brand name: it lists lot codes, UPC barcodes, best-by or use-by dates, establishment numbers (the “EST.” number inside the USDA mark on meat and poultry), model numbers or – for vehicles – model years and build dates. Compare them with what you have before you throw anything away.
Which agency: the FDA covers most food, medicines, supplements, cosmetics and medical devices; USDA's Food Safety and Inspection Service covers meat, poultry and processed egg products; the CPSC covers consumer products from toys to appliances; NHTSA covers vehicles, tires, child car seats and motor-vehicle equipment. FDA enforcement reports appear weekly and can list a recall several weeks after the company first announced it.
Recall questions
What products were recalled this week?
8 recalls were published by the FDA, USDA, CPSC and NHTSA in the last 7 days, 0 of them in the most serious category: 6 consumer products, 2 vehicles. The newest: Draeger recall: VentStar Resus Neo (Oct 7, 2026).
How do I know if a product I bought is recalled?
Search this page by brand or product name, then compare the lot code, UPC, best-by date or model number on your package with the identifiers on the recall page – a recall usually covers only certain lots or dates, not every product with that name. For a car, enter your 17-character VIN at nhtsa.gov/recalls.
What does Class I recall mean?
The FDA and USDA rate recalls by risk. Class I is the most serious: a reasonable probability that the product will cause serious health problems or death. Class II may cause temporary or reversible health problems; Class III is unlikely to cause harm.
Do I get my money back for a recalled product?
Usually yes. Food recalls ask you to throw the product away or return it to the store for a refund; CPSC recalls offer a free refund, repair or replacement; vehicle safety recalls are repaired free at a dealer. Each recall page shows the remedy the agency lists.
Recalls by type
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.