Drug Recalls
Recent drug recall reports from the FDA (US) and Health Canada, newest first. Each entry links to the full record -- product description, reason for recall, and severity classification -- refreshed daily.
Teva Pharmaceuticals USA, Inc
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit fo…
Teva Pharmaceuticals USA, Inc
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit fo…
VIONA PHARMACEUTICALS INC
Discoloration
Heritage Pharmaceuticals Inc
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals Inc
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals Inc
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals Inc
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals Inc
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals Inc
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Advanced Pharmaceutical Technology, Inc.
Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.
Church & Dwight Co., Inc.
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Aspiro Pharma Limited
Presence of Particulate Matter: Particulate matter identified as glass
AHCC
Product safety. Verify if your product is affected.Stop taking the product if you have milk allergy .Consult your healthcare provider for any health concerns.Co…
Acella Pharmaceuticals, LLC
Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.
Acuity Specialty Products, Inc.
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not…
Acuity Specialty Products, Inc.
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not…
Medline Industries, LP
Subpotent Drug
Dr. Reddy's Laboratories, Inc.
Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
Amlodipine 10 mg tablet
Product quality. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health co…
SV Labs Prescott Corporation
cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.
No7 Restore & Renew Face & Neck Multi Action Day Cream SPF 30
Other. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.Con…
Zydus Pharmaceuticals (USA) Inc
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
Zydus Pharmaceuticals (USA) Inc
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
ACME UNITED CORPORATION
Product Mix-up
Park Avenue Compounding
CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.