Device recall
Z-1222-2011: Maquet HEARTSTRING Aortic Cutter 4.3 mm, AC-3043, Lot numbers 9081071 and…
FDA device recall · Class II · Maquet Cardiovascular
Key facts
| Recall number (Z-number) | Z-1222-2011 |
|---|---|
| Recall event | 56860 |
| Product | Maquet HEARTSTRING Aortic Cutter 4.3 mm, AC-3043, Lot numbers 9081071 and 9082071, Manufactured by Maquet Cardiovascular, Wayne, New Jersey. Intended for use by cardiac surgeons during CABG procedures to create an opening in the wall of a vessel. |
| Product code | FZT |
| Recalling firm | Maquet Cardiovascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2011 |
| FEI number | 3000719698 |
At a glance
- None 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