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Browse Drug Recalls

8 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 8 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 8 FDA drug recalls.

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DateProductReasonClassFirm
Nov 6, 2024 MAXIM Assure Antibacterial, Chloroxylenol 0.1%, Net Contents: One U.S. Gallo... cGMP Deviations: Out of specification results for micro in hand soap products. Class II Midlab Incorporated
Nov 6, 2024 Genuine Joe Antibacterial Lotion Soap , Chloroxylenol 0.1%, 1 GALLON (3.78L),... cGMP Deviations: Out of specification results for micro in hand soap products. Class II Midlab Incorporated
Nov 6, 2024 Compliance Dishwashing Liquid & Antibacterial Soap, PCMX 0.1%, Net Contents: ... cGMP Deviations: Out of specification results for micro in hand soap products. Class II Midlab Incorporated
Nov 6, 2024 boardwalk ANTIBACTERIAL HANDSOAP REFILL, Chloroxylenol 0.1%, 1 gal. (3.78 L),... cGMP Deviations: Out of specification results for micro in hand soap products. Class II Midlab Incorporated
Nov 6, 2024 Array Liquid Antiseptic Handwash, Chloroxylenol 0.1%, NET CONTENTS: 128 FL OZ... cGMP Deviations: Out of specification results for micro in hand soap products. Class II Midlab Incorporated
Nov 6, 2024 ROYALAB Germ Away Antibacterial Hand Soap, Chloroxylenol 0.1%, NET CONTENTS: ... cGMP Deviations: Out of specification results for micro in hand soap products. Class II Midlab Incorporated
Aug 8, 2022 Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a)... CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride. Class II Midlab Incorporated
Aug 8, 2022 Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride ... CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride. Class II Midlab Incorporated

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.