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Browse Drug Recalls

54 FDA drug safety recalls.

FDA Drug Recall Enforcement Database

Browse 54 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 54 FDA drug recalls.

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DateProductReasonClassFirm
Jan 2, 2018 Ampicillin and Sulbactam for Injection 1.5 g vial, sterile Dry Powder for in... Presence of Particulate Matter: A confirmed customer report was received for the presence of visi... Class I Aurobindo Pharma Ltd.
Dec 20, 2017 Linezolid Injection 600 mg/300 mL (2 mg/mL), 300 mL Single-use, ready-to-use ... Presence of Particulate Matter; white particulate matter identified as mold was found in one bag Class I AuroMedics Pharma LLC
Dec 4, 2017 Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only,... Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) ... Class I AuroMedics Pharma LLC
Dec 16, 2016 Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only,... Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance. Class III Aurobindo Pharma USA 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.