FDA Devices recall · Reported January 28, 2015
Powered stretcher chair used during facial and eye surgeries. One chair per package.
The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.
TransMotion Medical Inc recalled Powered stretcher chair used during facial and eye surgeries. One chair per package. - a moderate-severity action.
Powered stretcher chair used during facial and eye surgeries. One chair per package. was recalled by TransMotion Medical Inc in January 28, 2015. Reason: The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.. Check the official notice for the remedy. Verify recall #Z-0996-2015 with the FDA Devices before acting.
The recall
TransMotion Medical Inc issued this moderate-severity FDA Devices recall-The firm is finding that the stretcher chair controllers are moving the chairs involuntarily..
- Moderate
- severity level
- 1K units
- affected scope
- Class II
- classification
- January 28, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0996-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0996-2015) was formally reported on January 28, 2015, with the manufacturer initiating the action on November 14, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. TransMotion Medical Inc is listed as the recalling firm, operating out of Sharon Center, OH. Federal records list the affected scope as 1,127 units.
The documented reason for this recall is: The firm is finding that the stretcher chair controllers are moving the chairs involuntarily. Distribution data in the federal record shows the product reached: Worldwide Distribution - US Distribution and the countries including Canada, Australia, Chile, China, Costa Rica, Germany, Algeria, Israel, Italy, South Korea, Malaysia, Nigeria, Netherlands, Poland, Portugal, Saudi Ara…. 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
Powered stretcher chair used during facial and eye surgeries. One chair per package.
Reason for recall
The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0996-2015 |
| Date reported | January 28, 2015 |
| Date initiated | November 14, 2014 |
| Recalling firm | TransMotion Medical Inc |
| Firm location | Sharon Center, OH |
| Affected scope | 1,127 units |
| Distribution | Worldwide Distribution - US Distribution and the countries including Canada, Australia, Chile, China, Costa Rica, Germany, Algeria, Israel, Italy, South Korea, Malaysia, Nigeria, Netherlands, Poland, Portugal, Saudi Arabia, Singapore, Thai… |
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-0996-2015) 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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Nationwide recalls with similar severity or category timing
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Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026