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

Recall Z-0852-2015 — GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 510(k) requirements. For use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and glassware are h

U.S. FDA — Device Enforcement · Sweden · 2014-11-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0852-2015
Date of alert
2014-11-26
Country / jurisdiction
Sweden
Risk level
Class II
Risk type
recall
Brand
Getinge Disinfection Ab
Product category
device
Product type
Devices
Reported risk: Getinge Disinfection AB received complaints regarding sediment residuals in the manifold of the washer and disinfector of Getinge 46-Series (CM302) with PACS 300/350 control. After performing detailed root cause analysis, the firm has identified the problem as insufficient water flow throughout the manifold due to formation of air pockets where sedimentation may occur.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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