TransMotion Medical — Class II medical device recall Z-0064-2017
Terminated recall by Winco Mfg., LLC, reported 2016-10-19, distributed in AR, CA, CO, CT, FL, GA, IL, KS…. Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.
| Recall number | Z-0064-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Winco Mfg., LLC, Ocala, FL, United States |
| Recall initiated | 2016-06-29 |
| Classified | 2016-10-09 |
| Reported by FDA | 2016-10-19 |
| Terminated | 2017-09-27 |
| Distributed | AR, CA, CO, CT, FL, GA, IL, KS, LA, MD, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, OK, PA, PR, RI, TN, TX, VA, WA, WI |
| Countries outside the US | AU, CA, CH, IT, PA, TW |
| Quantity | 264 stretcher |
Product
TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.
Reason for recall
Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.
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-0064-2017. 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.