Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2612-2017 — 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

U.S. FDA — Device Enforcement · United States · 2017-05-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2612-2017
Date of alert: 2017-05-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Z-Medica, LLC
Product category: device
Product type: Devices

Reported risk: Packaging breach may compromise sterility

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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