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.
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
An unrecoverable error may occur where a component will fail to complete the reboot cycle, become non-functional and must be replaced.
Inhibitory substance was detected.
Potential for metal in product
Inhibitory substance was detected.
Potential for metal in product
Potential for metal in product
Potential for metal in product
Sandwiches contain undeclared egg and milk.
Potential for metal in product
Microbial Contamination of Non-Sterile Products
Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually contain moxifloxacin 5 mg/mL
Defective Container: Customer complaints for leaking bottles and dispensing issues.
Subpotent
Hyundai Motor America (Hyundai) is recalling certain 2020-2021 Santa Fe, 2021 Sonata, and Elantra vehicles. During manufacturing, the windshield may not have been properly bonded to the…
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain JTEKT power steering gear assembly service parts for 2007-2021 Tundra and 2008-2022 Sequoia, part numbers 44250-0C160,…
Potential for open packaging seals compromising the sterility of the surgical gowns
Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and list its…
Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged with a label stating 6FR may contain a 7FR device and vice versa
The back of some Medical Device Identification Cards provided to patients were printed with an erroneous statement stating the following: "This patient has a complete MR conditional system…
Instructions for use were updated to include additional information to facilitate the selection and use of the collar device.
Firm is initiating a correction due to the possibility of fluid ingress. Fluid entering the device may short various electronic components thus leading to system shutdown, which could…
Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released…
Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released…
Browse recent months with enough recall history for useful comparison.
