Device recall
Z-0950-2025: Medical procedure kits labeled as: 1) ECONO STERILE STRABIS SCISS STR 4.5"STER…
FDA device recall · Class II · Sklar Instruments
Key facts
| Recall number (Z-number) | Z-0950-2025 |
|---|---|
| Recall event | 95946 |
| Product | Medical procedure kits labeled as: 1) ECONO STERILE STRABIS SCISS STR 4.5"STER 50, Model Number 96-2540; 2) ECONO STERILE STRABIS SCISS CVD 4.5"STER 50, Model Number 96-2541; 3) ECONO STERILE STRABIS SCISS STR 4.5"STER 25, Model Number 96-2542; 4) ECONO STERILE STRABISMUS SCISS STR4.5"CS/25, Model… |
| Product code | HNF |
| Recalling firm | Sklar Instruments |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2523865 |
At a glance
- None Linked 510(k)s
- 10–99 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