Device recall
Z-1252-2016: Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#…
FDA device recall · Class II · Innovative Ophthalmic Products, Inc
Key facts
| Recall number (Z-number) | Z-1252-2016 |
|---|---|
| Recall event | 73386 |
| Product | Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#: M3-175) GL-Single Plate 230mm2 (IOP reorder#: M3-230) |
| Product code | KYF |
| Recalling firm | Innovative Ophthalmic Products, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2016 |
| 510(k) numbers | K062252 |
| FEI number | 2083993 |
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