Some bottles may contain mixed strengths of the product.
Prescription Drugs
💊 Drugs • 11,927 recalls
Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02
TRIOVA PHARMACEUTICALS
Failed impurities/ degradation specifications: Out of specification for organic impurities.
Presence of Foreign Substance consistent with granules from desiccant packs used during storage
Some bottles may contain mixed strengths of the product.
NP Thyroid 30, Thyroid Tablets, USP, 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-329-01.
Acella Pharmaceuticals
Superpotent Drug.
Failed Dissolution Specification: The dissolution test at the 24 month time point (end of shelf life) yielded an out-of-specification result.
NP Thyroid 90, Thyroid Tablets, USP, 1 & 1/2 grain (90 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-331-01.
Acella Pharmaceuticals
Superpotent Drug.
Failed Dissolution Specifications
Failed dissolution specification: The dissolution test at the 24 month time point (end of shelf life) yielded an out of specification result.
Failed dissolution specifications
Lamotrigine Tablets, USP, 150 mg, 20,000-count bulk container, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA, For repackaging by: AvKare Inc., Pulaski, TN 38478, Bulk Shipment, NDC 59746-247-97.
Jubilant Cadista Pharmaceuticals
Presence of Foreign Substance visually consistent with the silica granules present in the desiccant packs utilized during storage of the product.
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
West-Ward Columbus
Failed Impurities/Degradation Specifications: Out of Specification for impurity 6 and total degradants.
Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 USA. NDC: 67457-187-50
Mylan Institutional
Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.
Failed dissolution specifications: Low stage 3 results obtained for dissolution during routine stability testing.
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins
Epinephrine Injection USP, 0.3 mg (Auto-Injector), 0.3 mg/ 0.3 mL pre-filled syringe, Rx Only, Manufactured for Teva Pharmaceuticals USA, Inc. North Wales, PA 19454. NDC 0093-5986-27
Teva Pharmaceuticals USA
CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.
Nizatidine Oral Solution, 15 mg/mL (75 mg/5mL) USP 480 mL bottles, Rx Only Distributed by: Gemini Laboratories, LLC Bridgewater, NJ 08807 NDC 60846-301-15
Amneal Pharmaceuticals of New York
CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.