Device recall
Z-1734-2017: POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-1734-2017 |
|---|---|
| Recall event | 76730 |
| Product | POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components. |
| Product code | OXQ |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 7, 2017 |
| FEI number | 3008403546 |
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