Device recall
Z-0710-2024: Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
FDA device recall · Class I · Maquet Cardiovascular, LLC
Key facts
| Recall number (Z-number) | Z-0710-2024 |
|---|---|
| Recall event | 93548 |
| Product | Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit |
| Product code | CAC |
| Recalling firm | Maquet Cardiovascular, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K201305 |
| 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