Device recall
Z-1255-2011: Face Tent Hospilak Ref. No. 110-E, Face Tent, Adult No Tubing, Manufactured for…
FDA device recall · Class II · Convatec Inc.
Key facts
| Recall number (Z-number) | Z-1255-2011 |
|---|---|
| Recall event | 57626 |
| Product | Face Tent Hospilak Ref. No. 110-E, Face Tent, Adult No Tubing, Manufactured for Unomedical inc. Hospilak Ref. No. 111-E, Face Tent, Adult No Tubing, with 15mm OD Connector Manufactured for Unomedical inc. Hospilak Ref. No. 115-E, Face Tent, Adult 5 (1.5m) Tubing Manufactured for Unomedical inc… |
| Product code | BYL |
| Recalling firm | Convatec Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 27, 2013 |
| FEI number | 3011987967 |
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