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.
Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between…
Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between…
Software: If the user excludes voxels from the Gamma calculation that are below a dose threshold (Suppress gamma calculation), the Gamma Passing Rate (GPR) calculated for individual ROIs is…
Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
Kits should contain Filter Straws with Standard Luer Connections however, the kits contain Filter Straws with Neuraxial connectors preventing interface with the other components of the kit.
Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products.
Product was made with a lack of proper pasteurization.
Illegible Label
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished RTE Sprig and Sprout Ham and Cotija Torta Sandwich on Telera Roll.
Undeclared wheat
Product was made with a lack of proper pasteurization.
Product was made with a lack of proper pasteurization.
Product was made with a lack of proper pasteurization.
Product was made with a lack of proper pasteurization.
Nissan North America, Inc. (Nissan) is recalling certain 2023 Rogue vehicles. The driver and front passenger seat belt pretensioners may have been incorrectly manufactured, which can cause…
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual…
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male…
Failed Impurities/Degradation Specification: Out of specification for organic impurities
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
CGMP Deviations: potential presence of Burkholderia cepacia complex
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Chemical Contamination; presence of benzene.
Labeling: Incorrect or Missing Package Insert
Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified…
Browse recent months with enough recall history for useful comparison.
