Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

COUMADIN FOR INJECTION (Warfarin Sodium for Injection Recalled by Bristol-Meyers Squibb Due to Presence of Particulate Matter: particulate matter identified as...

Date: May 12, 2014
Company: Bristol-Meyers Squibb
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Bristol-Meyers Squibb directly.

Affected Products

COUMADIN FOR INJECTION (Warfarin Sodium for Injection, USP 5 mg Single-Use Vial Rx Only Distributed by Bristol Meyers Squibb Company, Princeton, NJ 08543 USA NDC 0590-0324-96

Quantity: 50,724 Vials

Why Was This Recalled?

Presence of Particulate Matter: particulate matter identified as metallic-like and non-metallic cellulose fiber particles found in retain vials

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Bristol-Meyers Squibb

Bristol-Meyers Squibb has 1 total recall tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report