Device recall
Z-1239-04: Battery-operated Cautery High Temperature, fine/Loop/ Vasectomy Tip
FDA device recall · Class II · Aaron Medical Industries, Inc.
Key facts
| Recall number (Z-number) | Z-1239-04 |
|---|---|
| Recall event | 29487 |
| Product | Battery-operated Cautery High Temperature, fine/Loop/ Vasectomy Tip |
| Product code | HQP |
| Recalling firm | Aaron Medical Industries, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2012 |
| FEI number | 3007593903 |
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