Device recall
Z-0293-2016: Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis…
FDA device recall · Class II · TZ Medical Inc.
Key facts
| Recall number (Z-number) | Z-0293-2016 |
|---|---|
| Recall event | 72451 |
| Product | Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03 |
| Product code | FRO |
| Recalling firm | TZ Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 24, 2016 |
| 510(k) numbers | K071442 |
| FEI number | 1000127185 |
At a glance
- 1–9 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