95,094 total recalls in our database
Marquez Brothers International
Undeclared milk.
Marquez Brothers International
Undeclared milk.
Mondelez Global
Hard corn starch lumps were found in the product
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
Harrow Eye
Lack of Assurance of Sterility
B BRAUN MEDICAL
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
Premier Dental Products
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.
B BRAUN MEDICAL
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
B BRAUN MEDICAL
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Medline Industries
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries
Unapproved design changes to the products outside of the 510(k) clearance.
Unapproved design changes to the products outside of the 510(k) clearance.
Olympus Corporation of the Americas
Potential for detachment of a distal tip component of the device during use.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.