FDA Recall Terminated

Precise Digital Accelerator Intended to be used for radiation therapy treatments of malignant neoplastic diseases, as determined by a licensed medical practitioner.

Recall: Z-1088-2015 · Initiated January 7, 2015

Recall

Recall Number
Z-1088-2015
Event Number
70279
Firm
Elekta, Inc.
FEI Number
1037831
Product Code
IYE
Status
Terminated
Root Cause
Other
Initiated
January 7, 2015
Posted
February 10, 2015
Terminated
April 14, 2016
Address
400 Perimeter Center Ter Ne, Ste 50, Atlanta, GA, 30346-1227

Description

Precise Digital Accelerator Intended to be used for radiation therapy treatments of malignant neoplastic diseases, as determined by a licensed medical practitioner.

Reason

Elekta has identified a batch of securing bolts that fix the Gantry counter frame weight stack may fail.

Action

Elekta sent an Urgent Important Field Safety Notice on January 7, 2015, to all affected customers. Elekta recommended that customers replace the M20 x 50 MM bolts marked 'OF' on the gantry counterbalance frame immediately. The digital linear accelerator must not be used until these 'OF' bolts are replaced. Elekta recommended that customers put the machine in a parked position at 0, and attach the gantry locking straps. A Modification kit will be available as soon as possible which contains the correct bolts. Customers were instructed to complete the Important Field Safety Notice Acknowledgement form and return to their local Elekta Office or Representative. Customers with questions were instructed to contact their local Elekta representative. For questions regarding this recall call 404-993-5886.

Distribution

Worldwide Distribution - USA including AZ, CA, FL, KS, LA, MN, MO, NY, NC and Internationally to Austria, Bulgaria, Canada, China, Germany, Hungary, Italy, Malaysia, Malta, Netherlands, Norway, Russia, Spain, Sweden, Taiwan and Ukraine.

Quantity

46