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

Recall Z-0758-2013 — Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical transection of tissue during laparoscopic and open procedures. Model Numbers: NSLG2C14 NSLG2C25 NSLG2C35 NSLG2C45 NSLG2514 NSLG2S25 NSLG2S35 NSLGS545

U.S. FDA — Device Enforcement · United States · 2012-11-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0758-2013
Date of alert
2012-11-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ethicon Endo-Surgery Inc
Product category
device
Product type
Devices
Reported risk: Potential for self activation while the device is in use, which may result in unintended thermal damage.
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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