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

Recall Z-0492-2015 — Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet Ethicon LLC- Made in USA.

U.S. FDA — Device Enforcement · United States · 2014-10-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0492-2015
Date of alert
2014-10-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ethicon, Inc.
Product category
device
Product type
Devices
Reported risk: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black braid) meets the expected sterility assurance level for sterile products.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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