Device recall
Z-1595-05: OASIS Medical Vidaurri LASIK Flap Irrigator, Product Specification 4036V. The…
FDA device recall · Class II · Oasis Medical Inc
Key facts
| Recall number (Z-number) | Z-1595-05 |
|---|---|
| Recall event | 33431 |
| Product | OASIS Medical Vidaurri LASIK Flap Irrigator, Product Specification 4036V. The Vidaurri LASIK Flap Irrigator is a 16g x 1/2'' stainless steel cannula with two 25g x 9/16'' tip extensions. There are eight .25mm ports (four per tip). |
| Product code | KYG |
| Recalling firm | Oasis Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 24, 2014 |
| 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