Device recall
Z-2596-2014: Prime Care Transcend Mattress, Prime Care Transcend Perimeter Mattress, Prime…
FDA device recall · Class II · Primus Medical LLC
Key facts
| Recall number (Z-number) | Z-2596-2014 |
|---|---|
| Recall event | 68805 |
| Product | Prime Care Transcend Mattress, Prime Care Transcend Perimeter Mattress, Prime Care Transcend Advanced Mattress, Prime Care Transcend Advanced Perimeter Mattress, Prime Plus Bariatric Mattress and Prime Plus Bariatric Perimeter Mattress, individual units packaged seperately. Model Numbers: TCM3576… |
| Product code | FMW |
| Recalling firm | Primus Medical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 19, 2017 |
| FEI number | 3007538326 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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