Device recall
Z-1393-05: ''NAMIC Custom Angiographic Kit'' sold under the following labels: (1) Medical…
FDA device recall · Class III · Boston Scientific Corp
Key facts
| Recall number (Z-number) | Z-1393-05 |
|---|---|
| Recall event | 32288 |
| Product | ''NAMIC Custom Angiographic Kit'' sold under the following labels: (1) Medical University of South Carolina. Pouch Catalog # 60131481; (2) Covenant Medical Center, Pouch Catalog #60131603; (3) St. Joseph Hospital, Pouch Catalog #60101041; (4) Spectrum Health, Pouch Catalog #61020031 (5) Rush… |
| Product code | DTZ |
| Recalling firm | Boston Scientific Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 31, 2005 |
| 510(k) numbers | K782095 |
| 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