Ra Medical Systems recalls DABRA RA-308 Excimer Lasers with taller wheel mounting that may fall over, causing injury. Affected units have specific serial numbers listed in the recall.
Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury.
Ra Medical Systems is recalling DABRA RA-308 Excimer Lasers due to a taller wheel mounting that could cause the device to fall over, potentially injuring users or patients. This recall affects specific serial numbers listed in the notice.
The laser has a taller wheel mounting that could cause it to tip over during use. If it falls, it might injure the user or patient, especially in medical settings where the device is handled carefully.
Healthcare professionals using the DABRA RA-308 Excimer Laser for vascular procedures are most at risk. Patients receiving treatment with this device may also be affected.
Check the serial number on the device. Affected units have specific serial numbers listed in the recall notice, including RA00027, RA00039, and other numbers starting with RA000.
Look for the serial number on the device to confirm if it's in the list of affected units.
If your device has an affected serial number, stop using it immediately to prevent potential injury.
The laser has a taller wheel mounting that could cause it to fall over during use, potentially injuring users or patients.
Affected serial numbers include RA00027, RA00039, RA00046, RA00049, and others listed in the recall notice.
The recall notice does not specify a return process, so contact Ra Medical Systems directly for instructions.
We’ve drafted a message you can send Ra Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0050-2021 — Ra Medical Systems Ra Medical Systems Hello, I own a Ra Medical Systems that is covered by recall Z-0050-2021 from Ra Medical Systems. 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.
