PlainRecalls
FDA Devices Moderate Class II Ongoing

Phoroptor VRx Digital Refraction System Model Numbers: 16242

Reported: April 9, 2025 Initiated: February 28, 2025 #Z-1501-2025

Product Description

Phoroptor VRx Digital Refraction System Model Numbers: 16242

Reason for Recall

The head of the phoropter head could come loose and potentially detach due to a default in the assembly.

Details

Recalling Firm
Reichert, Inc.
Units Affected
1876 units
Distribution
Domestic: Nationwide Distribution. International: Austria, Bolivia, Canada, Denmark, France, Germany, Hong Kong, India, Israel, Italy, Morocco, Netherlands, Norway, Qatar, Saudi Arabia, Singapore, Slovakia, Switzerland, Thailand, United Arab Emirates, and United Kingdom.
Location
Depew, NY

Frequently Asked Questions

What product was recalled?
Phoroptor VRx Digital Refraction System Model Numbers: 16242. Recalled by Reichert, Inc.. Units affected: 1876 units.
Why was this product recalled?
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 9, 2025. Severity: Moderate. Recall number: Z-1501-2025.