Device recall
Z-1869-2016: Laparotomy Pack Latex Free, part number 007725-7. This is a custom convenience…
FDA device recall · Class II · Windstone Medical Packaging, Inc.
Key facts
| Recall number (Z-number) | Z-1869-2016 |
|---|---|
| Recall event | 73743 |
| Product | Laparotomy Pack Latex Free, part number 007725-7. This is a custom convenience surgical instrument disposable kit. There are multiple component in this kit and the recalled item subject to recall is Medtronic Kerlix X-Ray Detectable Laparotomy Sponges. |
| Product code | LRS |
| Recalling firm | Windstone Medical Packaging, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 16, 2016 |
| FEI number | 1000125955 |
At a glance
- None 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