Complete FDA and NHTSA recall records dated in 2025, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their…
Sample probes with defective probe tips, when used with clinical chemistry analyzers, may lead to a lower concentration being dispensed, which may not be detectable by QC checks, which…
It was determined that the consumable issue may result in No Call - INT CTL 1 and/or False Negative results on a small portion of the lot of test cartridges.
Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel.
A new software update (v1.20) is introducing error codes for the Dxl 9000 which prevents the assay from being performed and a delay in results from being generated, and may require field…
Recent post-market surveillance data suggests a possible association of higher microbial contamination levels from TJF duodenoscopes when manual cleaning was delayed beyond one hour and a…
The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential to exhibit interrupted motion on the display screen, caused by a software…
Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
A manufacturing defect in the sample probe (S probe). The corners of the tip of the defective S probe are rounded and chamfered, which can prevent the proper formation of the "air layer"…
Due to printing quality, label does not declare Egg allergen clearly.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Due to printing quality, label does not declare these allergens clearly: Egg, Milk, Soy.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Post process damage to containers, potential for microbial growth, swollen and or exploding containers
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Due to printing quality, label does not declare these allergens clearly: Egg and Milk.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
Listeria Monocytogenes detected on food contact surfaces in Ready To Eat sandwich manufacturer facility.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
