Device recall
Z-0137-2024: Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of…
FDA device recall · Class II · Maquet Cardiovascular, LLC
Key facts
| Recall number (Z-number) | Z-0137-2024 |
|---|---|
| Recall event | 93085 |
| Product | Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a sternotomy incision approach. Product Code: OM-10000Z |
| Product code | MWS |
| Recalling firm | Maquet Cardiovascular, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2242352 |
At a glance
- None 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