LEASEIR recalls MHR XCELL surgical laser devices with missing DANGER label on console. This safety issue requires immediate attention to prevent potential injury during use.
The console label for affected devices is missing the "DANGER" symbol.
LEASEIR is recalling its MHR XCELL surgical laser devices because the console label lacks the required DANGER symbol. This missing safety label could lead to improper use and potential injury during procedures like hair removal or skin treatments.
The console label missing the DANGER symbol means users might not recognize the device's high-risk nature. This could lead to improper handling, especially during procedures involving intense light pulses that target hair follicles and blood vessels.
Surgical professionals and patients using the LEASEIR MHR XCELL laser devices for hair removal or skin treatments. Those with the specific model MHR 110-b software version 1.5.0.0 are most at risk.
Check for the model number MHR 110-b and software version 1.5.0.0 on the device. The missing DANGER label on the console is the key indicator of the recalled item.
Look for the DANGER symbol on the console; if missing, the device is part of the recall.
The missing DANGER label means users might not recognize the device's high-risk nature, potentially leading to improper handling during procedures.
Check the console label for the DANGER symbol; if missing, contact LEASEIR for guidance on next steps.
The recall indicates the device is not safe to use as the missing label could lead to improper handling and potential injury.
We’ve drafted a message you can send LEASEIR to request your refund or repair — edit it as you like.
Subject: Recall Z-1130-2026 — LEASEIR LEASEIR Hello, I own a LEASEIR that is covered by recall Z-1130-2026 from LEASEIR. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
