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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
Feb 10, 2026 Adbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single d... Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lo... Class II LEO PHARMA INC
Jan 19, 2017 Calcipotriene Cream 0.0005%, packaged in a) 60g tube, (NDC 66993-877-61), b) ... Incorrect/Undeclared excipients: inadvertent omission of a drug excipient from the the Authorized... Class II LEO PHARMA INC
Jan 16, 2017 Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension, ... Labeling: Incorrect or missing package insert: the affected product was packaged with an out-of-... Class III LEO 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.