Device recall
Z-1021-05: EMCEE OBTURATOR (7F) for use with 8F Sheath, REF #92580008, packaged in…
FDA device recall · Class III · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1021-05 |
|---|---|
| Recall event | 32286 |
| Product | EMCEE OBTURATOR (7F) for use with 8F Sheath, REF #92580008, packaged in individual labeled pouches, 10 units per box, 40 boxes per case. Firm on label: Schneider/NAMIC, Glens Falls, New York 12801 |
| Product code | DYB |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 21, 2005 |
| 510(k) numbers | K9805040 |
| FEI number | 3017892510 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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