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

Recall Z-1062-2022 — 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS VIDEO-CYSTO-URETHROSCOPE REV; 11272VU 11272VUK CMOS VIDEO-CYSTO-URETHROSCOPE US; 11272VUA 11272VUAK CMOS VIDEO-CYSTO-URETHROSCOPE US

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-1062-2022
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)
4048551313350
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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.