Device recall
Z-2250-2015: Medical Device Exchange Angio-Seal VIP Platform/Vascular Closure Device 6F…
FDA device recall · Class II · EXP Pharmaceutical Services Corp
Key facts
| Recall number (Z-number) | Z-2250-2015 |
|---|---|
| Recall event | 71608 |
| Product | Medical Device Exchange Angio-Seal VIP Platform/Vascular Closure Device 6F; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 610130. EXP (repackager), St. Jude Medical (OEM) Device, hemostasis, vascular |
| Product code | MGB |
| Recalling firm | EXP Pharmaceutical Services Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 30, 2015 |
| FEI number | 3004376386 |
At a glance
- None Linked 510(k)s
- 10–99 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