Device recall
Z-1371-05: Tri-Plex Adapter, single unit (MD-04000)or box of 25 (MD-04001) or case of 100…
FDA device recall · Class II · Medical Device Group Inc.
Key facts
| Recall number (Z-number) | Z-1371-05 |
|---|---|
| Recall event | 32468 |
| Product | Tri-Plex Adapter, single unit (MD-04000 )or box of 25 (MD-04001) or case of 100 (MD-04002). Sterile. Single Use. |
| Product code | MOD |
| Recalling firm | Medical Device Group Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 6, 2012 |
| 510(k) numbers | K010401 |
| FEI number | 3004500043 |
At a glance
- 1–9 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