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

Recall Z-0465-2014 — Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue.

U.S. FDA — Device Enforcement · United States · 2013-11-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0465-2014
Date of alert
2013-11-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Karl Storz Endoscopy America Inc
Product category
device
Product type
Devices
Reported risk: KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the 33821WTD Wavy grasper was mislabeled as 33821DYD Axillent Debakey Grasping Forceps.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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