Flexicare recalls BritePro Solo Mini laryngoscopes with Pro Miller Blade Size 1.5 due to potential handle illumination failure. Affected units sold July-2020 to Dec-2020.
Laryngoscope handles may not illuminate as intended.
Flexicare is recalling BritePro Solo Mini laryngoscopes with Pro Miller Blade Size 1.5 because the handle may not illuminate properly. This could affect medical procedures requiring clear visibility during surgery.
The laryngoscope handle may not illuminate as intended, which could reduce visibility during medical procedures. This might make it harder for healthcare providers to see the throat area clearly.
Healthcare professionals using the BritePro Solo Mini laryngoscope with Pro Miller Blade Size 1.5 are affected. Those who use the device for medical procedures are most at risk.
Check for the product name 'BritePro Solo Mini' with Pro Miller Blade Size 1.5. Affected units were sold between July 2020 and December 2020 with reference numbers starting with 040-02-0415U.
Verify the product name and reference number on the device to confirm if it's affected.
The recall states the handle may not illuminate as intended, but it does not indicate a risk of serious injury or death. This is a low-risk issue.
Check for the product name 'BritePro Solo Mini' with Pro Miller Blade Size 1.5 and reference numbers starting with 040-02-0415U sold between July 2020 and December 2020.
The recall does not specify a remedy, so no action is required beyond checking if your device is affected.
We’ve drafted a message you can send Flexicare Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2184-2025 — Flexicare Medical Flexicare Medical Hello, I own a Flexicare Medical that is covered by recall Z-2184-2025 from Flexicare Medical. 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.
