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Browse Drug Recalls

3 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 3 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 3 FDA drug recalls.

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DateProductReasonClassFirm
Oct 20, 2023 DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers, Original, 4... Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer produc... Class II Omega & Delta Co., Inc.
Oct 20, 2023 DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers, 8FL OZ (237... Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer produc... Class II Omega & Delta Co., Inc.
Oct 20, 2023 Equate Hand Sanitizer (Ethyl Alcohol 62%), 7.5 FL.OZ. (221 mL) UPC 6 81131 ... Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer produc... Class II Omega & Delta Co., 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.