Device recall
Z-1570-2023: M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and…
FDA device recall · Class II · New Wave Endo-Surgical, Corp.
Key facts
| Recall number (Z-number) | Z-1570-2023 |
|---|---|
| Recall event | 92005 |
| Product | M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall |
| Product code | HCF |
| Recalling firm | New Wave Endo-Surgical, Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 2, 2024 |
| FEI number | 3015209038 |
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