Device recall
Z-1340-2011: Walcott Rx Products, Surgical Division, Corneal Marking Pad, REF RX40490…
FDA device recall · Class II · Aspen Surgical Products, Inc.
Key facts
| Recall number (Z-number) | Z-1340-2011 |
|---|---|
| Recall event | 57792 |
| Product | Walcott Rx Products, Surgical Division, Corneal Marking Pad, REF RX40490, Sterile. For use in ophthalmic surgery. |
| Product code | HMR |
| Recalling firm | Aspen Surgical Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2011 |
| FEI number | 3002750084 |
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