Reichert Phoroptor VRx Digital Refraction System Model Numbers: 16241 recall — FDA Z-1500-2025
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Overview of recall records associated with Reichert, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 3.
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Phoroptor VRx Head may detach from the bracket that connects the Phoroptor VRx Head to an ophthalmic stand. If the Phoroptor VRx Head detaches from the bracket, it can fall onto a patient…
This page summarizes recall records in which the official source identifies Reichert, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.