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Browse Drug Recalls

5 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 5 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 5 FDA drug recalls.

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DateProductReasonClassFirm
Oct 12, 2021 Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60... Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actua... Class I Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Sep 28, 2021 Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC... Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on ... Class III Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Sep 28, 2021 Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC:... Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on ... Class III Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Jan 27, 2021 Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 636... Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolact... Class I Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Jan 27, 2021 Spironolactone Tablets, USP, 50 mg, packaged in 30-count bottles, Rx only, Ma... Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolact... Class II Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

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.