FDA Recall
Terminated
Lumbar Extension Machine for Physical Therapy
Recall: Z-0935-2015
·
Initiated December 3, 2013
Recall
- Recall Number
- Z-0935-2015
- Event Number
- 69422
- Firm
- MedX Holdings, Inc.
- FEI Number
- 1051095
- Product Code
- ISD
- Status
- Terminated
- Root Cause
- Unknown/Undetermined by firm
- Initiated
- December 3, 2013
- Posted
- January 7, 2015
- Terminated
- September 29, 2016
- Address
- 839 Nw 25th Ave, Ocala, FL, 34475-5789
Description
Lumbar Extension Machine for Physical Therapy
Reason
Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
Action
Medx began contacting its consignees December 30, 2013, to schedule testing on the devices at their facility. The technician has been scheduled to complete required testing of these devices in the field. For questions regarding this recall call 322-351-2005.
Distribution
Worldwide Distribution - USA including MO, IL, ID, and MN and Internationally to Germany and South Korea.
Quantity
9