Device recall
Z-2063-2012: Stryker Neptune Bronze Rover, Part 0700-007-000 Neptune Bronze Rover Waste…
FDA device recall · Class I · Stryker Instruments Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2063-2012 |
|---|---|
| Recall event | 61747 |
| Product | Stryker Neptune Bronze Rover, Part 0700-007-000 Neptune Bronze Rover Waste Management System Instructions For Use. Intended for use in the surgical environment or physician's office to collect and dispose of surgical fluid waste. |
| Product code | FYD |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 23, 2016 |
| 510(k) numbers | K012991 |
| FEI number | 1811755 |
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