RecallDepth

Varian Medical Systems, Flexible Probe with Blocking Water, GM11002420, (Part of the Segmented Cylinder Set, GM11004150)

This recall has been terminated (originally issued November 23, 2011).

Company
Varian Medical Systems, Inc.
Recall Initiated
May 20, 2010
Posted
November 23, 2011
Terminated
December 5, 2011
Recall Number
Z-0282-2012
Quantity
81 parts
Firm Location
Charlottesville, VA
Official Source
View on FDA website ↗

Reason for Recall

The Instructions For Use ( IFU) distributed with product prior to 2004 lacks the correct limit to the sterilization cycles and checks regarding the firm seating of the blocking washer.

Distribution

Worldwide Distribution: USA, Germany, Belgium, Canada, Mexico City, Spain, Brazil, Switzerland, Uzbekistan, India

Lot / Code Info

Lot number Y01 to E19

Root Cause

Labeling Change Control

Action Taken

Varian Medical Systems sent a Medical Device Recall (PNL-GM-42697-2) in May 2010 for the blocking washer on the flexible probe, Varian part number GM11002420, a component of the Segmented Cylinder Applicator Set. The letter was to inform users that a flexible probe with an unstable or shifted blocking washer must not be used due to the potential for treatment length error. The blocking washer may move from rough handling or sterilization. Users were told to discard any instances of the obsolete Instructions for Use (IFU) in use and replace it with the IFU (PGM11004150 4 March 24, 2010.pdf). A Receipt Verification Card was included requesting consignees to fill out, fax or e-mail immediately to Varian BrachyTherapy.

More recalls by Varian Medical Systems, Inc.

View all recalls by this company →