Complete FDA and NHTSA recall records dated in 2026, 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.
Certain lots of product have the potential for a sterile barrier breach.
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may…
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Presence of a Foreign Substance; black particles observed in liquid
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Presence of particulate matter: a white thread-like structure in the cartridge
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
Potential contamination with Salmonella.
Potential contamination with Salmonella.
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Potential contamination with Salmonella.
Potential contamination with Salmonella.
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.
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.
