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

Recall Z-1061-2022 — CYSTO-URETHRO-FIBERSCOPE REF 11272C1 CYSTOSCOPE, 15FR X 370MM, ADULT REF 11272C2 and Kit Number 11272CK2 CYSTO-URETHRO-FIBERSCOPE REF 11272CU1 and Kit Number 11272CUK1

U.S. FDA — Device Enforcement · United States · 2022-04-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1061-2022
Date of alert
2022-04-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Karl Storz Endoscopy
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4048551226100
Reported risk: Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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