Device recall
Z-0493-05: VERSAPOINT, Hysteroscopic system Connector Cable, Non-Sterile, Reusable (20 uses…
FDA device recall · Class II · Ethicon, Inc
Key facts
| Recall number (Z-number) | Z-0493-05 |
|---|---|
| Recall event | 30711 |
| Product | VERSAPOINT, Hysteroscopic system Connector Cable, Non-Sterile, Reusable (20 uses only). US Distribution/Manufactured for GYNECARE, A division of Ethicon, Inc., a Johnson & Johnson Company, Somerville, NJ 08876. The product subject of this recall is the connector cable which goes between the… |
| Product code | HIH |
| Recalling firm | Ethicon, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 31, 2005 |
| 510(k) numbers | K962482 |
| FEI number | 2210968 |
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