Device recall
Z-1019-04: Monarc Subfascial Hammock With Tensioning Suture, Product Number 72403830/1
FDA device recall · Class III · American Medical Systems
Key facts
| Recall number (Z-number) | Z-1019-04 |
|---|---|
| Recall event | 29142 |
| Product | Monarc Subfascial Hammock With Tensioning Suture, Product Number 72403830/1 |
| Product code | FTL |
| Recalling firm | American Medical Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 22, 2004 |
| 510(k) numbers | K023516 |
| FEI number | 1000116179 |
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