Device recall
Z-0403-2022: Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
FDA device recall · Class II · Maquet Cardiovascular, LLC
Key facts
| Recall number (Z-number) | Z-0403-2022 |
|---|---|
| Recall event | 89119 |
| Product | Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890 |
| Product code | MAL |
| Recalling firm | Maquet Cardiovascular, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 28, 2024 |
| 510(k) numbers | K954848 |
| FEI number | 2242352 |
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