NeuroLogica recalls medical flat panel digital x-ray imagers (model GMR40, serials 00001-00016) due to potential foot injury during backward transport of retrofit equipment.
While transporting the portable machine with the retrofit equipment in a backwards motion, there is potential for foot injury from the underside of the detector bin of the retrofit unit.
NeuroLogica is recalling medical flat panel x-ray imagers (model GMR40, serial numbers 00001-00016) because moving the device backward with retrofit equipment could cause foot injuries from the detector bin. This is a safety issue for medical staff who transport the equipment.
The hazard occurs when the portable x-ray machine is moved backward with retrofit equipment attached. The detector bin's underside could then cause foot injuries to anyone in close proximity during this movement.
Medical professionals who use or transport these x-ray imagers are most at risk, particularly during backward movement of the retrofit equipment.
Check for medical flat panel x-ray imagers with model number GMR40 and serial numbers from 00001 to 00016. These were sold with retrofit equipment for medical use.
Identify if your x-ray imager has model number GMR40 and serial numbers 00001 through 00016.
Ensure you do not move the equipment backward with retrofit equipment attached when transporting it.
Model number GMR40 with serial numbers 00001 through 00016.
Check for model number GMR40 and serial numbers 00001 through 00016 on the device.
The recall does not provide a specific remedy; check with NeuroLogica for guidance.
We’ve drafted a message you can send NeuroLogica to request your refund or repair — edit it as you like.
Subject: Recall Z-1391-2018 — NeuroLogica NeuroLogica Hello, I own a NeuroLogica that is covered by recall Z-1391-2018 from NeuroLogica. 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.
