Device recall
Z-1132-2008: Keeler All Pupil II Indirect Ophthalmoscope, Keeler Instruments, Inc., Broomall…
FDA device recall · Class II · Keeler Instruments Inc
Key facts
| Recall number (Z-number) | Z-1132-2008 |
|---|---|
| Recall event | 46741 |
| Product | Keeler All Pupil II Indirect Ophthalmoscope, Keeler Instruments, Inc., Broomall, PA 19008 |
| Product code | HLI |
| Recalling firm | Keeler Instruments Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2008 |
| 510(k) numbers | K854244 |
| FEI number | 2519784 |
At a glance
- 1–9 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