Class I - Dangerous
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
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Drugs Recalls
Prescription and over-the-counter medications
17,302 Total Recalls
Class I - Dangerous
Failed Impurities/Degradation - Out-of-specification results for Fluocinolone Acetonide impurity.
Class I - Dangerous
Labeling Not Elsewhere Classified: Ibuprofen Oral Suspension is missing dosing cups.
Class I - Dangerous
Failed Dissolution Specification
Class I - Dangerous
Failed Dissolution Specification
Class I - Dangerous
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
Class I - Dangerous
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
Catapres (clonidine hydrochloride, USP) 0.1 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0006-01
Boehringer Ingelheim Pharmaceuticals
Class I - Dangerous
An extraneous peak was observed for dissolution testing.
N-A-C (N-Acetyl-L-Cysteine, 500 mg, 100 capsules; Veggie Caps, white HDPE bottle with RED label Product # 107002 UPC: 790011070023
Jarrow Formulas
Class I - Dangerous
Mislabeling of SUS (N-A-C Sustain 600 mg 100 tab) with N-A-C N-Acetyl-L-Cysteine 500 mg, 100 cap.
Class I - Dangerous
SUBPOTENT DRUG
Catapres (clonidine hydrochloride, USP) 0.2 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0007-01
Boehringer Ingelheim Pharmaceuticals
Class I - Dangerous
An extraneous peak was observed for dissolution testing.
Catapres (clonidine hydrochloride, USP) 0.3 mg, tablet, 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877, Made in Germany, NDC, 0597-0011-01
Boehringer Ingelheim Pharmaceuticals
Class I - Dangerous
An extraneous peak was observed for dissolution testing.
Class I - Dangerous
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
NP Thyroid 15,Thyroid Tablets, USP 1/4 grain (15 mg) 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005, NDC 42192-327-01
Acella Pharmaceuticals
Class I - Dangerous
Subpotent Drug: FDA analysis found these products to be less than the labeled claim for the levothyroxine (T4) portion of the product.
Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution, 1 gallon (3785 mL) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, NDC 74484-002-04, UPC 7401037203427.
Genesis Partnership Company SA
Class I - Dangerous
CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.
Class I - Dangerous
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Class I - Dangerous
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Class I - Dangerous
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.
Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd., Shanghai, 200245, China for Sandoz Inc. Princeton, NJ 08540, NDC 0781-6172-22
eVenus Pharmaceutical Laboratories
Class I - Dangerous
DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.
Class I - Dangerous
Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.