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 7 of 30
Product may contain undeclared sugar.
Reported Oct 7, 2026 · H-1397-2026
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Reported Oct 7, 2026 · H-1405-2026
Potential Salmonella contamination.
Reported Oct 7, 2026 · H-1403-2026
This recall was initiated due to potential Salmonella contamination in diced jalape¿no received from the supplier
Reported Oct 7, 2026 · H-1398-2026
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Reported Oct 7, 2026 · H-1409-2026
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Reported Oct 7, 2026 · H-1408-2026
Undeclared Yellow 5 & 6, Red 3, and Blue 1
Reported Oct 7, 2026 · H-0001-2027
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Reported Oct 7, 2026 · H-1406-2026
Undeclared allergen ingredient (fish)
Reported Oct 7, 2026 · H-1400-2026
Undeclared shellfish (crab shell): source of ingredient Glucosamine sulfate
Reported Oct 7, 2026 · H-1401-2026
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
Reported Oct 7, 2026 · H-1404-2026
Microbial contamination of topical product.
Reported Oct 7, 2026 · D-0879-2026
Defective Container; packets were found to be either empty or partially full.
Reported Oct 7, 2026 · D-0873-2026
Lack of Assurance of Sterility
Reported Oct 7, 2026 · D-0874-2026
Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.
Reported Oct 7, 2026 · D-0875-2026
Discoloration: consumer complaints received for discolored tablets
Reported Oct 7, 2026
Failed dissolution specifications.
Reported Oct 7, 2026 · D-0877-2026
Microbial contamination of topical product.
Reported Oct 7, 2026 · D-0878-2026
Crystallization
Reported Oct 7, 2026 · D-0876-2026
Failed Dissolution Specifications: below specification
Reported Oct 7, 2026 · D-0010-2027
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-0004-2027
Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.
Reported Oct 7, 2026 · Z-3228-2026
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-3309-2026
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-0022-2027
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-0037-2027
Due to blood-to-glycol leak in the heat exchanger.
Reported Oct 7, 2026 · Z-3327-2026
Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, which if used could lead to infection.
Reported Oct 7, 2026 · Z-3305-2026
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.
Reported Oct 7, 2026 · Z-3277-2026
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation
Reported Oct 7, 2026 · Z-3325-2026
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-0060-2027