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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 10,701–10,720 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Dexamethasone Sodium Phosphate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Bumetadine all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Glycopyrrolate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Nicardipine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Phenylephrine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Heparin sodium all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Oxytocin all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Gentamicin Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Vancomycin HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Cefazolin all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Methohexital Sodium all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Lorazepam HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Fentanyl Citrate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Sufentanil Citrate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Early Baby TPN (Neonatal) all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Early TPN (Neonatal) all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

NICU STARTER TPN all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Ofirmev (Acetaminophen) injection all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Recall initiated
February 22, 2017
Reported by FDA
May 31, 2017
Distribution
U.S. Nationwide

View recall →

Drug Recall Ongoing Historical recordClass II

Ventolin HFA (albuterol sulfate) Inhalation, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20.

by GlaxoSmithKline, LLC

Reason
Defective Delivery System: Elevated number of units with out of specification results for leak rate
Recall initiated
May 16, 2017
Reported by FDA
May 31, 2017
Distribution
Nationwide in the US and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass II

Refresh Tears (Carboxymethylcellulose Sodium Solution) 0.5%, Lubricant Eye Drops, Sterile packaged as 1) two 15 mL bottles, USPC Code 784190442214, 2) 4x15 mL and one 5 mL bonus bottles, USPC Code 069886941746, Distributed by Cell Distributors, Union, NJ

by Cell Distributors

Reason
Labeling: Not elsewhere classified; product labeling lacks a NDC number, net weight information and does not contain the Drug Facts Panel.
Recall initiated
April 3, 2017
Reported by FDA
May 31, 2017
Distribution
Nationwide

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.