Device recall
Z-0066-2017: TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair. Intended use…
FDA device recall · Class II · Winco Mfg., LLC
Key facts
| Recall number (Z-number) | Z-0066-2017 |
|---|---|
| Recall event | 74922 |
| 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. |
| Product code | FPP |
| Recalling firm | Winco Mfg., LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2017 |
| FEI number | 1027229 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database