FDA Devices recall · Reported January 14, 2015
Lumbar Extension Machine for Physical Therapy
Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
MedX Holdings, Inc. recalled Lumbar Extension Machine for Physical Therapy - a moderate-severity action.
Lumbar Extension Machine for Physical Therapy was recalled by MedX Holdings, Inc. in January 14, 2015. Reason: Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devic…. Check the official notice for the remedy. Verify recall #Z-0935-2015 with the FDA Devices before acting.
The recall
MedX Holdings, Inc. issued this moderate-severity FDA Devices recall-Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devic….
- Moderate
- severity level
- 9 units
- affected scope
- Class II
- classification
- January 14, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0935-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0935-2015) was formally reported on January 14, 2015, with the manufacturer initiating the action on December 3, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. MedX Holdings, Inc. is listed as the recalling firm, operating out of Ocala, FL. Federal records list the affected scope as 9.
The documented reason for this recall is: Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing. Distribution data in the federal record shows the product reached: Worldwide Distribution - USA including MO, IL, ID, and MN and Internationally to Germany and South Korea.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0935-2015 |
| Date reported | January 14, 2015 |
| Date initiated | December 3, 2013 |
| Recalling firm | MedX Holdings, Inc. |
| Firm location | Ocala, FL |
| Affected scope | 9 |
| Distribution | Worldwide Distribution - USA including MO, IL, ID, and MN and Internationally to Germany and South Korea. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0935-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Methodology · Corrections · Archive as of August 2026