Reported Apr 9, 2025 · Ongoing
Phoroptor VRx Digital Refraction System Model Numbers: 16241
Reichert, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Reichert, Inc. · 3362 Walden Ave · Depew, NY · 14043-2437
Is this the product you have?
- Phoroptor VRx
- Digital Refraction System Model Numbers16241
- Lot codes and dates
- Model Numbers(1) 16241
- UDI-DI(1) 00812559011716
- Serial NumbersTBD
- NoteThe majority of units within the scope of the planned recall are older devices which do not have a UDI on the label
- Amount recalled
- 122 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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