Device recall
Z-0272-2010: Richard Wolf Hulka Clip; for single patient use only; a sterile tubal occluding…
FDA device recall · Class II · Richard Wolf Medical Instruments Corp.
Key facts
| Recall number (Z-number) | Z-0272-2010 |
|---|---|
| Recall event | 53586 |
| Product | Richard Wolf Hulka Clip; for single patient use only; a sterile tubal occluding device; 2 clips per procedure tray/pouch, 10 pouches per shipping carton; Richard Wolf Medical Instruments Corp., Vernon Hills, IL 60061; item 4986.90. Indicated for use for female sterilization (permanent contraception)… |
| Product code | HGB |
| Recalling firm | Richard Wolf Medical Instruments Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 16, 2011 |
| PMA numbers | P870080 |
| FEI number | 1418479 |
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