DrugAug 25, 2021
Teva Pharmaceuticals USA Methylprednisolone Acetate Injectable Suspension USP, 80 mg/mL recall — FDA D-0743-2021
Lack of Assurance of Sterility
Class IIFDA: TerminatedTeva Pharmaceuticals USA
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 116
10,685 detailed records are currently available in this category.
DrugAug 25, 2021
COMBIPATCH (ESTRADIOL/NORETHINDRONE ACETATE TRANSDERMAL SYSTEM) Combipatch recall — FDA D-0725-2021
Failed Stability Specifications; out of specification for shear.
Class IIFDA: OngoingNoven Pharmaceuticals Inc.
DrugAug 25, 2021
GAVILYTE - C GaviLyteTM - C PEG-3350 (240g) and Electrolytes for Oral Solution, USP with recall — FDA D-0726-2021
Failed Stability Specification; Out of specification for Osmolarity
Class IIFDA: TerminatedNovel Laboratories, Inc. d.b.a LUPIN
DrugAug 25, 2021
Teva Pharmaceuticals USA Haloperidol Decanoate Injection 100 mg/mL recall — FDA D-0732-2021
Lack of Assurance of Sterility
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugAug 25, 2021
DuPont Nutrition USA Avicel, Mirocrystalline cellulose recall — FDA D-0728-2021
Out of specification results for conductivity.
Class IIIFDA: TerminatedDuPont Nutrition USA, Inc.
DrugAug 25, 2021
Teva Pharmaceuticals USA Alprostadil Injection USP, 500 mg/mL, 1 mL single dose, vials, 5 mL recall — FDA D-0742-2021
Lack of Assurance of Sterility
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugAug 25, 2021
Carvedilol Tablets, USP 25 mg, 500 Tablets bottles recall — FDA D-0753-2021
Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were found in the bottle
Class IIFDA: TerminatedZydus Pharmaceuticals (USA) Inc.
DrugAug 25, 2021
High Performance Formulas Cholestene capsules, 1200 mg of red yeast rice per 2 capsules recall — FDA D-0727-2021
Marketed Without an Approved NDA/ANDA
Class IIFDA: TerminatedHigh Performance Formulas, LLC (HPF, LLC)
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL-CLONIDINE HCL PF INJECTABLE 21 mL recall — FDA D-0709-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL-FENTANYL PF INJECTABLE 21 mL syringe recall — FDA D-0711-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Ethosuximide Oral Solution USP 250 mg/5 mL, 16 fl oz (473 mL) recall — FDA D-0723-2021
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Class IIFDA: TerminatedPAI Holdings, LLC. dba Pharmaceutical Associates Inc.
DrugAug 18, 2021
Eli Lilly & Company Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use recall — FDA D-0720-2021
cGMP deviations: Atypical appearance, decrease in size and change in color of the lyophilized cake of drug product.
Class IIFDA: TerminatedEli Lilly & Company
DrugAug 18, 2021
SUN PHARMACEUTICAL INDUSTRIES Venlafaxine Tablets, USP 50 mg*, 100 Tablets recall — FDA D-0703-2021
Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL-BACLOFEN PF INJECTABLE 21 mL syringes recall — FDA D-0708-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Med Shop Total Care MORPHINE-BUPIVACAINE PF INJECTABLE 21 mL, 22 mL, 23 mL, 41 mL and 43 mL recall — FDA D-0710-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
PAI Holdings, LLC. dba Pharmaceutical Associates Cimetidine Hydrochloride Oral Solution 300 recall — FDA D-0722-2021
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Class IIFDA: TerminatedPAI Holdings, LLC. dba Pharmaceutical Associates Inc.
DrugAug 18, 2021
Med Shop Total Care HYDROMORPHONE HCL-BUPIVACAINE HCL PF INJECTABLE 21 and 22 mL syringes in recall — FDA D-0717-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 18, 2021
Nystatin Oral Suspension, USP 100,000 units per mL, Cherry/Peppermint Flavor recall — FDA D-0721-2021
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Class IIFDA: TerminatedPAI Holdings, LLC. dba Pharmaceutical Associates Inc.
DrugAug 18, 2021
Med Shop Total Care MORPHINE-BUPIVACAINE-KETAMINE PF INJECTABLE 21 mL syringe in two recall — FDA D-0713-2021
Non-Sterility
Class IFDA: TerminatedMed Shop Total Care Inc.
DrugAug 11, 2021
Cascade Kelly Holdings Global Hand Sanitizer with moisturizer, Alcohol-based Antiseptic 80% recall — FDA D-0698-2021
CGMP Deviations: Does not meet monograph for denaturant.
Class IIFDA: TerminatedCascade Kelly Holdings LLC
DrugAug 11, 2021
Cascade Kelly Holdings Global Hand Sanitizer with moisturizer, Alcohol-based Antiseptic 80% recall — FDA D-0697-2021
CGMP Deviations: Does not meet monograph for denaturant.
Class IIFDA: TerminatedCascade Kelly Holdings LLC
DrugAug 11, 2021
Qikmoov Vy&Tea recall — FDA D-0749-2021
Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.
Class IFDA: OngoingQikmoov LLC
DrugAug 11, 2021
Chantix (varenicline)Tablets, Contains: 1 Starting Week (0.5 mg* x 11 tablets), 3 Continuing recall — FDA D-0700-2021
CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs acceptable interim acceptable intake limit
Class IIFDA: OngoingPfizer Inc.
DrugJul 28, 2021
Scentsational Soaps & Candles Goose Creek Hand Sanitizer aloe Watermelon Lemonade recall — FDA D-0682-2021
Chemical contamination: product found to be contaminated with methanol (wood alcohol), benzene and acetaldehyde.
Class IFDA: TerminatedScentsational Soaps & Candles Inc.
How to use this drug recall index
A drug recall record can include the reason for recall, firm, status, distribution pattern, quantity and FDA classification. This site does not provide medical advice; it organizes public recall information and links users back to official sources.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
What the database can and cannot tell you
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.