The latest food, drug and medical device recalls reported by the U.S. Food and Drug Administration, newest first. Data updated Oct 21, 2026.
87,918 recalls · page 12 of 30
Reported Oct 7, 2026 · Z-3306-2026
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
Reported Oct 7, 2026 · Z-0023-2027
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
Reported Oct 7, 2026 · Z-0064-2027
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
Reported Oct 7, 2026 · Z-0041-2027
Due to incorrect inside packaging label for eyepiece.
Reported Oct 7, 2026 · Z-3333-2026
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.
Reported Oct 7, 2026 · Z-3314-2026
Undeclared Egg Allergen
Reported Sep 30, 2026 · H-1395-2026
Contamination with Listeria monocytogenes
Reported Sep 30, 2026 · H-1396-2026
Potential contamination with pesticides.
Reported Sep 30, 2026 · H-1393-2026
Potential Wheat Kernel contamination.
Reported Sep 30, 2026 · H-1391-2026
Potential Wheat Kernel contamination.
Reported Sep 30, 2026 · H-1392-2026
Product may contain foreign material: small stones and other hard objects.
Reported Sep 30, 2026 · H-1394-2026
Salmonella
Reported Sep 30, 2026 · H-1390-2026
Potential Listeria contamination from dripping condensation in cooler.
Reported Sep 30, 2026 · H-1389-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0860-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0863-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0871-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0855-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0862-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0856-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0858-2026
Defective Delivery System: Possibility of no medication in the prefilled pen.
Reported Sep 30, 2026 · D-0868-2026
Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification.
Reported Sep 30, 2026 · D-0867-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0861-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0857-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0870-2026
Lack of Assurance of Sterility
Reported Sep 30, 2026 · D-0859-2026
cGMP Deviations
Reported Sep 30, 2026 · D-0854-2026
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
Reported Sep 30, 2026 · Z-3247-2026
Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.
Reported Sep 30, 2026 · Z-3229-2026