Device recall
Z-0762-04: VasoSeal ES, Extravascular Security Vascular Closure Device, Catalog No. 76000…
FDA device recall · Class III · Datascope Collagen Products Division
Key facts
| Recall number (Z-number) | Z-0762-04 |
|---|---|
| Recall event | 28389 |
| Product | VasoSeal ES, Extravascular Security Vascular Closure Device, Catalog No. 76000. Class III (PMA P920004), sterile (via gamma irradiation) device is sold in cardboard shelf cartons containing 5 ea. individual kits. The individual kits are packaged in a blister with Tyvek lid within a heat sealed foil… |
| Product code | MGB |
| Recalling firm | Datascope Collagen Products Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 6, 2004 |
| PMA numbers | P920004 |
| FEI number | 3003071194 |
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