Storz Equipment, Fluid Management Stand, for Fluid Management Systems, Product Number 26601EQ-KT
FDA Recall Z-0144-2008 · Posted 2007-11-07
Recalling FirmKarl Storz Endoscopy America Inc
Recall StatusTerminated
Product CodeHIG
Date Initiated2007-08-17
Date Terminated2012-02-29
Product Quantity287
Reason for Recall
Outflow Difference: The accuracy of the Equimat displayed value could be influenced by external factors of the cart/stand and may result in a fluctuating or inaccurate reading.
Firm Action
All affected customers were notified via a Customer Letter issued on September 10, 2007 via FedEx overnight mail. The letter describes the problem with the device and the health hazard risk, and provides instructions for users to return the old stand and make arrangements for replacement stands.
Root Cause
Device Design
Distribution Pattern
Nationwide
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.