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

Electrode, Cutting, 24FR, 0.30MM (27040G-.30/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives). — recall Z-1315-2013

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-1315-2013
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.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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