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Browse Drug Recalls

106 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 106 FDA drug recall enforcement actions. Each entry includes the product description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Drug Safety Recalls

Browse 106 FDA drug recalls.

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DateProductReasonClassFirm
Jan 12, 2023 Allopurinol Tablets USP, 100 mg, 100-count bottle, Rx Only, Manufactured for:... Presence of Foreign Substance: Presence of a small piece of green plastic embedded in the crack t... Class II Accord Healthcare, Inc.
Nov 29, 2022 Daptomycin for Injection 350 mg/vial 1 Single-dose vial, Rx only, Manufacture... Labeling mixup: cartons labeled as Daptomycin 350 mg/vial were found to contain vials of Daptomyc... Class I Accord Healthcare, Inc.
Jan 28, 2021 Glycopyrrolate Injection, USP 0.4 mg/2 mL (0.2 mg/mL) 25 x 2 mL Single Dose V... Labeling; Label Mix-up; correctly labeled 2 mL vials were packaged into blister strips labeled fo... Class III Accord Healthcare, Inc.
Jul 27, 2020 Hydrochlorothiazide 50mg tablets, 14-count bags, Rx only, Distributed by: Cal... CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent po... Class II Calvin Scott & Company, Inc.
Aug 21, 2018 Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufact... Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets US... Class I Accord Healthcare, Inc.
Dec 20, 2016 Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord... Failed tablet/capsule specification: missing break line on the 5mg tablet. Class II Accord Healthcare, Inc.

Frequently Asked Questions

When a drug safety issue is identified — through FDA inspections, laboratory testing, adverse event reports, or manufacturer quality checks — the responsible company issues a recall to remove the affected products from the market. Pharmacies pull the product from shelves, and consumers are advised to contact their healthcare provider for alternatives.

The leading causes include cGMP deviations, impurity contamination (including nitrosamines like NDMA), failed dissolution or stability testing, sterility issues, potency problems, labeling errors, and foreign particle contamination.

Use the search and filter tools on this page to look up specific medications, active ingredients, or manufacturers. Each recall entry includes the product description, lot numbers, and distribution details.