Device recall
Z-0298-2017: Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to…
FDA device recall · Class II · TZ Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0298-2017 |
|---|---|
| Recall event | 74809 |
| Product | Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and provide hemostasis for lacerations, abrasions, vascular access sites and following surgical incision. It can be used to achieve hemostasis at the skin surface for arterial/venous… |
| Product code | FRO |
| Recalling firm | TZ Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 28, 2016 |
| 510(k) numbers | K040208 |
| 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