FDA Device recall Z-0066-2017
TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair
- FDA Device
- Class II
- terminated
- Published 2016-10-19
On 2016-10-19 the FDA classified a Class II recall of TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair by Winco Mfg, citing non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0066-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-29 |
| Published | 2016-10-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Winco Mfg |
| Distribution | 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 |
Product
TransMotion Medical, TMM5 Series Mobile Surgical 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
Non-conforming component caused arms of TMM4 Stretcher chair to no longer meet design specifications.
Identifiers
| code_info | All identified serial numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0066-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.