Drug recall
Phoroptor VRx Digital Refraction System Model Numbers: 16241
FDA recall event 96266 · Class II · Reichert, Inc.
Key facts
| Event ID | 96266 |
|---|---|
| Recall numbers | Z-1500-2025, Z-1501-2025 |
| Recalling firm | Reichert, Inc. |
| Product type | Devices |
| Products | Phoroptor VRx Digital Refraction System Model Numbers: 16241, Phoroptor VRx Digital Refraction System Model Numbers: 16242 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The head of the phoropter head could come loose and potentially detach due to a default in the assembly. |
| Initiation date | Feb 28, 2025 |
| Report date | Apr 9, 2025 |
| City | Depew |
| State | NY |
| Country | United States |
| FEI number | 1000159913 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: