Device recall
Z-0742-2007: Disposable Bimanuals Irrigation and Aspiration Handpiece Set: Item #1721…
FDA device recall · Class II · Oasis Medical Inc
Key facts
| Recall number (Z-number) | Z-0742-2007 |
|---|---|
| Recall event | 38120 |
| Product | Disposable Bimanuals Irrigation and Aspiration Handpiece Set: Item #1721 Disposable Bimanuals Irrigation/Aspiration Set 21 Gauge, Dual Port; Item #1721-A - Disposable Bimanual Aspiration Handpiece 21g; Item #1721-I Disposable Bimanuals Irrigation/Aspiration Set, 21g, Open End; Item #1721-S… |
| Product code | KYG |
| Recalling firm | Oasis Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2011 |
| FEI number | 2083373 |
At a glance
- None 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