Reichert recalls Phoropt: VRx Digital Refraction System model 16241 due to risk of head detachment during use. Affected units lack UDI labels and may require replacement.
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Reichert is recalling its Phoroptor VRx Digital Refraction System model 16241 because the phoropter head could become loose and detach. This poses a risk of injury during eye exams if the device is not properly secured.
The phoropter head could become loose and detach due to a manufacturing defect in the assembly. If the head detaches during an eye exam, it could cause injury to the user or patient.
Optometrists and eye care professionals who use the Phoroptor VRx Digital Refraction System model 16241 are affected. Those with older units lacking UDI labels are at higher risk.
Check for model number 16241 on the device. Older units without a UDI label (unique device identifier) are included in this recall.
Look for model number 16241 on the device label.
Contact Reichert directly for replacement or repair options.
No, but you should check if your device is affected and contact Reichert for next steps.
The model number is 16241.
Yes, the majority of recalled units are older devices without a UDI label.
We’ve drafted a message you can send Reichert to request your refund or repair — edit it as you like.
Subject: Recall Z-1500-2025 — Reichert Reichert Hello, I own a Reichert that is covered by recall Z-1500-2025 from Reichert. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
