Device recall
Z-1071-2013: Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to…
FDA device recall · Class II · J T Posey Company
Key facts
| Recall number (Z-number) | Z-1071-2013 |
|---|---|
| Recall event | 63622 |
| Product | Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to limit a patient's movement to the extent necessary for treatment or protection of the patient or others. |
| Product code | FMQ |
| Recalling firm | J T Posey Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2014 |
| FEI number | 3016004577 |
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