FDA Device recall Z-0936-2015
Cervical Extension Machine for Physical Therapy
- FDA Device
- Class II
- terminated
- Published 2015-01-14
On 2015-01-14 the FDA classified a Class II recall of Cervical Extension Machine for Physical Therapy by Medx Holdings, citing review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0936-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-03 |
| Published | 2015-01-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medx Holdings |
| Distribution | ID, IL, MN, MO |
Product
Cervical 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.
Identifiers
| code_info | Serial Numbers: 02511166, 02511167, 02511171, 02511170. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0936-2015%22
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