Complete FDA and NHTSA recall records dated in February 2024.
These records include useful source details for the selected month.
Water filter may have been assembled incorrectly, resulting in unfiltered tap water being used for reprocessing. This may expose a patient to a potentially contaminated device, presenting a…
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
Rotating adaptor O-ring manufacturing defect impacting seal integrity which may lead to a leak during infusion of medication.
Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to…
The expiration date is missing from the primary (inner) packaging. The secondary (outer) box label correctly states the expiration date of February 12, 2033, for this lot
Their is a potential for false positive results when using Pneumonia panel.
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
Incorrect component descriptions within the "Contents" section on the Tyvek lid for individual kit trays.
There is an issue with the Access Ultrasensitive Insulin assay protocol file (APF) for use with the DxI 9000 Access Immunoassay Analyzer (APF 182 test definition version 6.7 and below). The…
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
Devices may not be rendered sterile due to an internal gap that may be present on some devices causing increased difficulty cleaning prior to steam sterilization. There is an increased risk…
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
Amount of Phosphatidyl Serine in product is less than stated on the label
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
Undeclared allergen, wheat, from not declaring sub-ingredients of enriched flour.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
