Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may compromise sterility...
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 Z-Medica, LLC directly.
Affected Products
QuikClot TraumaPad, , sterile, soft, white, X-ray detectable hemostatic dressing Part Number 460 Manufactured by Z-Medica, LLC 4 Fairfield Boulevard, Wallingford, CT 06492 USA For use as a topical dressing for local management of bleeding wounds such as cuts, lacerations, and abrasions. It may also be used for temporary treatment of severely bleeding wounds such as surgical wounds (operative, postoperative, dermatological, etc.) and traumatic injuries
Quantity: 2910 pieces
Why Was This Recalled?
Packaging breach may compromise sterility
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Z-Medica, LLC
Z-Medica, LLC has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report