DrugApr 21, 2021
LITE NFOAMY HEALTHCARE PERSONNEL HANDWASH Lite'n Foamy Healthcare Personnel Handwash recall — FDA D-0364-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 123
10,685 detailed records are currently available in this category.
DrugApr 21, 2021
TRESIBA FlexTouch recall — FDA D-0619-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
INSULIN DILUTING MEDIUM FOR NOVOLOG NovoLog (Insulin aspart) Injection, 100 units/mL recall — FDA D-0616-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
Antiseptic Hand Cleaner (Chloroxylenol, 1.0%), Net Contents: 1 US Gallon/ 3.79 Liters per recall — FDA D-0361-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 21, 2021
Spartan Chemical Co Lite'n Foamy Lemon Blossom Hand Sanitizer recall — FDA D-0359-2021
Microbial Contamination of Non-Sterile Products; lot tested positive for Bulkholderia multivorans
Class IFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 21, 2021
TRESIBA FlexTouch recall — FDA D-0621-2021
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the…
Class IFDA: TerminatedNovo Nordisk Inc.
DrugApr 21, 2021
LITE NFOAMY EUCALYPTUS MINT SANITIZING HANDWASH Lite'n Foamy Eucalyptus Mint Sanitizing recall — FDA D-0363-2021
CGMP Deviations
Class IIFDA: TerminatedSpartan Chemical Co Inc.
DrugApr 14, 2021
Metformin HCl Extended-Release Tablets, USP, 500 mg recall — FDA D-0325-2021
Failed Moisture Limits: Out of specification for water content
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugApr 14, 2021
Washington Homeopathic Products Sp-4, 100 mL solution bottles recall — FDA D-0322-2021
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Class IIIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugApr 14, 2021
Washington Homeopathic Products LCL-2-0191, 5 gallon carboys recall — FDA D-0323-2021
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Class IIIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugApr 14, 2021
Washington Homeopathic Products Macula Pellets Homeopathic Medicine, 1 Oz bottles recall — FDA D-0321-2021
An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.
Class IIIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugApr 14, 2021
Kimberly-Clark Scott Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz) recall — FDA D-0319-2021
Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are incorrectly labeled as Moisturizing Foam Hand Sanitizer
Class IIFDA: TerminatedKimberly-Clark Corporation
DrugApr 14, 2021
Guanfacine Extended-Release Tablets 2 mg,100-count bottles recall — FDA D-0324-2021
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
Class IIFDA: OngoingApotex Corp.
DrugApr 7, 2021
Ferring Pharmaceuticals ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use recall — FDA D-0318-2021
Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
Class IIFDA: TerminatedFerring Pharmaceuticals Inc.
DrugApr 7, 2021
Ferring Pharmaceuticals ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use recall — FDA D-0317-2021
Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
Class IIFDA: TerminatedFerring Pharmaceuticals Inc.
DrugApr 7, 2021
Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01, For Intravenous recall — FDA D-0315-2021
Crystallization: customer complaints for crystallization in finished product.
Class IFDA: TerminatedZydus Pharmaceuticals (USA) Inc.
DrugApr 7, 2021
Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01, For Intravenous recall — FDA D-0316-2021
Crystallization: customer complaints for crystallization in finished product.
Class IFDA: TerminatedZydus Pharmaceuticals (USA) Inc.
DrugMar 31, 2021
SODIUM CHLORIDE 0.9% SODIUM CHLORIDE Irrigation, USP 1000 mL Semi-Rigid Bottle recall — FDA D-0313-2021
Presence of particulate matter.one confirmed customer report of particulate matter within two semi-rigid bottles identified prior to use
Class IIFDA: TerminatedICU Medical Inc.
DrugMar 31, 2021
Adams.Secret.co Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs recall — FDA D-0311-2021
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Class IFDA: TerminatedAdams.Secret.co
DrugMar 31, 2021
Golden State Medical Supply Omeprazole Delayed Release Capsules, USP, 20 mg, 1000-count recall — FDA D-0312-2021
Failed Impurities/Degradation Specifications: Out of Specification results obtained for unknown impurities during stability testing by manufacturer
Class IIFDA: TerminatedGolden State Medical Supply Inc.
DrugMar 31, 2021
Adams.Secret.co Adam's Secret Extra Strength 1500, 800 mg, 10 count blister packs recall — FDA D-0310-2021
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Class IFDA: TerminatedAdams.Secret.co
DrugMar 24, 2021
Bryant Ranch Prepack, Inc. dba BRP Spironolactone Tablets, USP, 50 mg recall — FDA D-0304-2021
Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.
Class IIFDA: OngoingBryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
DrugMar 24, 2021
Akorn Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per recall — FDA D-0301-2021
Failed Impurities/Degradation Specifications; out of specification for unknown impurity observed during 6 month stability testing
Class IIFDA: TerminatedAkorn, Inc.
DrugMar 24, 2021
Breckenridge Pharmaceutical Omeprazole Delayed-Release Capsules, USP, 20 mg, 1000 count recall — FDA D-0308-2021
Failed Impurities/Degradation Specifications: Out-of-Specification results obtained for unknown impurities during stability testing.
Class IIFDA: TerminatedBreckenridge Pharmaceutical, 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.