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Browse Drug Recalls

11 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 11 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 11 FDA drug recalls.

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DateProductReasonClassFirm
Dec 12, 2024 Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, M... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Dec 12, 2024 Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, In... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Dec 12, 2024 Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufacture... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Dec 12, 2024 Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma,... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Dec 12, 2024 Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactur... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Dec 12, 2024 Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactur... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Dec 12, 2024 Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufact... Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID. Class III Akron Pharma, Inc.
Oct 15, 2024 OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Lax... CGMP Deviations Class II Akron Pharma, Inc.
Feb 17, 2023 DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Ph... Labeling: Incorrect or Missing Lot and/or Exp Date Class III Akron Pharma, Inc.
Aug 4, 2022 Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-802... Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet. Class III Akron Pharma, Inc.
Aug 4, 2022 Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle ... Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet. Class III Akron Pharma, 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.