Device recall
Z-1461-2008: Alcon/Grieshaber Morris ILM Forceps, Direct Action; Manual ophthalmic surgical…
FDA device recall · Class III · Alcon Research, Ltd
Key facts
| Recall number (Z-number) | Z-1461-2008 |
|---|---|
| Recall event | 47401 |
| Product | Alcon/Grieshaber Morris ILM Forceps, Direct Action; Manual ophthalmic surgical instrument, Catalog Number: 641.22; Non-sterile/Reusable; Alcon Laboratories, Inc., Fort Worth, TX 76134. |
| Product code | HNR |
| Recalling firm | Alcon Research, Ltd |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 18, 2008 |
| FEI number | 1610287 |
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