Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile…
During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the…
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
Knee and Humeral socket implants contain incorrect labeling.
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Uneviscerated Fish
Water was bottled under insanitary conditions.
Listeria monocytogenes
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Ingredients List declares peanut but the Contains statement does not declare peanut
Water was bottled under insanitary conditions.
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Potential contamination with Salmonella.
Product contains undeclared cyclamates.
Product contains undeclared cyclamates.
Water was bottled under insanitary conditions.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Browse recent months with enough recall history for useful comparison.
