Reichert recalls Phoroptor VRx Digital Refraction System Model 16242 due to potential head detachment. Affected units lack UDI labels; check serial numbers for recall.
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Reichert is recalling Phoropt: VRx Digital Refraction System Model 16242 because the head could become loose and detach during use. This poses a risk of injury if the head separates while the device is in operation.
The phoropter head could become loose due to a manufacturing defect in the assembly. If the head detaches while the device is in use, it could cause injury to the user or patient.
Optometrists and opticians who use the Phoroptor VRx Digital Refraction System Model 16242 are most at risk. Patients using the device may also be affected if the head detaches.
Check for model number 16242 on the device. Most affected units lack a UDI label, so look for serial numbers or other identifiers as noted in the recall notice.
Look for model number 16242 on the device or its packaging.
Contact Reichert, Inc. for further instructions if you own the recalled device.
The head of the phoropter could become loose and detach due to a default in the assembly.
Check for model number 16242. Most affected units lack a UDI label.
Contact Reichert, Inc. for further instructions.
We’ve drafted a message you can send Reichert to request your refund or repair — edit it as you like.
Subject: Recall Z-1501-2025 — Reichert Reichert Hello, I own a Reichert that is covered by recall Z-1501-2025 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.
