Device recall
Z-0817-2019: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm…
FDA device recall · Class II · Angiotech (Manan Medical Products, Inc.)
Key facts
| Recall number (Z-number) | Z-0817-2019 |
|---|---|
| Recall event | 81968 |
| Product | Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm 14MTWX x 12.5 cm |
| Product code | DWO |
| Recalling firm | Angiotech (Manan Medical Products, Inc.) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2020 |
| 510(k) numbers | K890925 |
| FEI number | 1417485 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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