FDA Recall Terminated

Precedence System; SYST,PRECEDENCE, 16 SLICE 5/8 Manufactured by Philips Medical Systems (Cleveland), Inc. 595 Miner Road, Cleveland, OH 44143. The SKYLight Gamma Camera System is intended to product images depicting the anatomical distributions of single photon and positron emitting radioisotopes within the human body for interpretation by medical personnel.

Recall: Z-0255-2012 · Initiated September 27, 2011

Recall

Recall Number
Z-0255-2012
Event Number
60021
Firm
Philips Medical Systems
FEI Number
1525965
Product Code
KPS
Status
Terminated
Root Cause
Device Design
Initiated
September 27, 2011
Posted
November 19, 2011
Terminated
December 21, 2012
Address
3860 N 1st St, San Jose, CA, 95134-1702

Description

Precedence System; SYST,PRECEDENCE, 16 SLICE 5/8 Manufactured by Philips Medical Systems (Cleveland), Inc. 595 Miner Road, Cleveland, OH 44143. The SKYLight Gamma Camera System is intended to product images depicting the anatomical distributions of single photon and positron emitting radioisotopes within the human body for interpretation by medical personnel.

Reason

A mechanical malfunction of the button on the hand controller on the Philips Precedence and SKYLight SPECT systems may get stuck and cause unintended motion of a detector.

Action

Philips Medical Systems sent a "Customer Information" letter dated September 27, 2011 to all affected customers. The letter describes the product, problem, and the actions to be taken by the customers. The letter lists additional precautions the customers should use while operating the device. Philips will notify customers for replacing the affected product through an Action for Performance-Proactive Field Change Order to resolve the issue. Contact Philips Customer Care Solutions at 1-800-722-9377, option 5, for questions concerning this notice.

Distribution

Worldwide Distribution-USA (nationwide) including Puerto Rico.

Quantity

658 - all units in recall