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

Recall Z-0826-2015 — WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.

U.S. FDA — Device Enforcement · United States · 2014-12-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0826-2015
Date of alert
2014-12-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: The manufacturing dates and expiration dates were transposed on the Tyvek label.
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.

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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.