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.
Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case…
Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Customers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is expired and…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case…
Due to labeling error. Product incorrectly labeled.
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
May be contaminated with fluid from a reach truck
Product is likely Canola Oil, not Extra Virgin Olive Oil
May be contaminated with fluid from a reach truck
May be contaminated with fluid from a reach truck
Potential to be contaminated with Listeria monocytogenes
Label declares Shelled Edamame but does not specify or declare soy.
May be contaminated with fluid from a reach truck
May be contaminated with fluid from a reach truck
May be contaminated with fluid from a reach truck
Product may contain foreign objects of metal origin.
Undeclared milk
Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)
cGMP deviations
cGMP deviations
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.
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.
