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

Recall Z-1305-2013 — Electrode, cutting, 24FR (27050G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).

U.S. FDA — Device Enforcement · United States · 2009-06-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1305-2013
Date of alert
2009-06-01
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: Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.
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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