Lumbar Extension Machine for Physical Therapy — Class II medical device recall Z-0935-2015
Terminated recall by MedX Holdings, Inc., reported 2015-01-14, distributed in ID, IL, MN, MO. Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these device
| Recall number | Z-0935-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MedX Holdings, Inc., Ocala, FL, United States |
| Recall initiated | 2013-12-03 |
| Classified | 2015-01-07 |
| Reported by FDA | 2015-01-14 |
| Terminated | 2016-09-29 |
| Distributed | ID, IL, MN, MO |
| Countries outside the US | DE, KR |
| Quantity | 9 |
| Serial numbers | 01531278, 01531279, 01531280, 01531281, 01531282, 01531283, 01531284, 01531287, 01531288 |
Product
Lumbar Extension Machine for Physical Therapy
Reason for recall
Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0935-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.