GammaMed Plastic Needle with Mandrin; 2.0mm diameter, length 200 mm. Remote controlled radionuclide applicator system. V

FDA device recall Z-2992-2011 · posted 2011-08-10 · Terminated

Recall details

Recalling firm

Varian Medical Systems, Inc. Oncology Systems

Reason for recall

Needle tip may separate from the needle shaft such that the tip may detach in the patient upon withdrawal.

Action taken

Varian sent an "Urgent Medical Device Correction/Urgent Field Safety Notice" letter dated July 13, 2011 to all possibly affected customers. This notification supplements and modifies the previous "Customer Technical Bulletins" originally sent in September 2008. The initial Customer Technical Bulletins informed customers of the possibility that needle tips cans crack and separate. It also reminded users that the product has a limited life and to check needles prior to use as per instructions. Current correction notice letter instruct customers to stop using any plastic needles in inventory with lot numbers C01 to D01 and those with lot numbers starting with H or I. The letter also request that the recalled products be returned to Varian BrachyTherapy for replacement. The letters include information as to where the lot number is located on the device. All appropriate personnel should be notified of the correction notice. Contact information is provided for all geographical areas. USA contact for questions or concerns is 1-800-360-7909.

Root cause

Device Design

Status

Terminated

Product code

JAQ

Quantity affected

601 - all sizes.

Distribution

Worldwide Distribution - USA (nationwide) and the countries of: Argentina, Austria, Bangladesh, Belgium, Brazil, Canada, Columbia, Cyprus, Czech Republic Denmark, Dominican Republic, Estonia, France,

Date initiated

2011-07-13

Date posted

2011-08-10

Date terminated

2012-06-20

Location

Palo Alto, CA

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