Lubricant Eye Drops
Non-Sterility
Every FDA drug recall whose status is still Ongoing: the firm is still removing product from the market, or the FDA has not yet closed the file. Some were opened years ago and never formally terminated, so check the initiation date as well as the status.
2,760 recalls, newest first.
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Non-Sterility
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the container is a 0.5mL single-use syringe instead of a 5 mL dropper
MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with metformin and glyburide
Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen
Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen
Failed Tablets/Capsules specifications; missing/broken/extra tablets within the capsules
Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine