Drug Recalls — FDA Recall Database

10,690drug recall records

953FDA Class I records

8firms with 5+ records

Aidapak Services, LLC537 records

Database records

Records — page 239

10,690 detailed records are currently available in this category.

DrugJul 5, 2017

L. Perrigo Company Walgreens Daytime and Nighttime Cold & Flu recall — FDA D-0925-2017

Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the…

Class IIIFDA: TerminatedL. Perrigo Company

DrugJul 5, 2017

Sanofi-Aventis U.S Gaviscon recall — FDA D-0926-2017

Superpotent Drug: high out-of-specification result for magnesium.

Class IIIFDA: TerminatedSanofi-Aventis U.S. LLC

DrugJul 5, 2017

Minivelle recall — FDA D-0923-2017

Defective Delivery System: Out of specification for peel force from the release liner specification during stability testing at 18M 25C/60%RH.

Class IIIFDA: TerminatedNoven Pharmaceuticals, Inc.

DrugJul 5, 2017

American Pharmaceutical Ingredients Doxycycline Hyclate USP, active pharmaceutical recall — FDA D-0927-2017

Labeling: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.

Class IIFDA: TerminatedAmerican Pharmaceutical Ingredients LLC

DrugJun 28, 2017

Lucid Pharma Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg recall — FDA D-0921-2017

Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.

Class IIFDA: TerminatedLucid Pharma LLC

DrugJun 28, 2017

Vi-Jon Magnesium Citrate Saline Laxative Cherry Flavored recall — FDA D-0922-2017

Presence of foreign substance: glass particle

Class IIFDA: TerminatedVi-Jon, Inc.

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 7 mMol 100 mL Bag recall — FDA D-0913-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP, Service Code recall — FDA D-0916-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 7.5 mMol 100 mL Bag recall — FDA D-0909-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.75g in 300 mL 0.9% Sodium Chloride Injection USP recall — FDA D-0915-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

American Pharmaceutical Ingredients ESTRONE USP recall — FDA D-0919-2017

cGMP Deviations; lack of quality assurance.

Class IIFDA: TerminatedAmerican Pharmaceutical Ingredients LLC

DrugJun 21, 2017

Bausch & Lomb NasalCrom (cromolyn sodium) Nasal Spray, USP, 5.2 mg per spray, 200 metered recall — FDA D-0899-2017

CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.

Class IIFDA: TerminatedBausch & Lomb, Inc.

DrugJun 21, 2017

Pharmedium Services Potassium CHLORide added to 0.9% Sodium Chloride, 30mEq 100 mL Bag recall — FDA D-0906-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 10 mMol 100 mL Bag recall — FDA D-0911-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium CHLORide added to 0.9% Sodium Chloride, 10mEq 100 mL Bag recall — FDA D-0907-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate in 0.5% Dextrose, 7.5 mMol in 100 mL, Service Code recall — FDA D-0908-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 15 mMol 100 mL Bag recall — FDA D-0910-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.5g in 300 mL 0.9% Sodium Chloride Injection USP recall — FDA D-0914-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 20 mMol 100 mL Bag recall — FDA D-0912-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 14, 2017

Qualgen Estradiol 20 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count and 12 recall — FDA D-0891-2017

CGMP deviations- Lack of Quality Assurance

Class IIFDA: TerminatedQualgen

DrugJun 14, 2017

Qualgen Estradiol 12.5 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 recall — FDA D-0894-2017

CGMP deviations- Lack of Quality Assurance

Class IIFDA: TerminatedQualgen

DrugJun 14, 2017

Zenatane (isotretinoin) Capsules, USP, 20 mg, 30-count recall — FDA D-0884-2017

Failed Dissolution Specifications: out of specification results observed for low dissolution.

Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.

DrugJun 14, 2017

Qualgen Estradiol 10 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 recall — FDA D-0895-2017

CGMP deviations- Lack of Quality Assurance

Class IIFDA: TerminatedQualgen

DrugJun 14, 2017

Spectrum Laboratory Products Estradiol recall — FDA D-0881-2017

CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current…

Class IIFDA: TerminatedSpectrum Laboratory Products, 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.

Drug Recalls in the United States

Records — page 239

How to use this drug recall index

What the database can and cannot tell you