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.
Incorrect software flagging may occur for the assay that may potentially lead to an erroneous result.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
There is a potential for the sterility of the device to be compromised.
There is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used.
IVX Station Reconstitution Transfer Sets were shipped in advance of the IVX Station upgrade and not intended for clinical use but are engineering devices intended for use during set up and…
Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the…
Due to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This…
Undeclared allergen (milk not listed as sub ingredient of butter). Milk also not listed in 'Contains' statement.
Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.
Undeclared soy flour
The product is in violation for not having an approved filed process and for not having monitoring records.
Product contaminated with elevated levels of coliform.
Undeclared allergens (soy, milk) and Yellow #5
BMW of North America, LLC (BMW) is recalling certain 2025 X3 30 xDrive vehicles. The front brake discs may have been damaged during transport before they were installed on the vehicle.
Chemical contamination: Presence of benzene
Lack of Assurance of Sterility: Media fill with bacterial contamination
Cross Contamination
Presence of Particulate Matter
Chemical contamination: Presence of benzene
Browse recent months with enough recall history for useful comparison.
