Flexicare Medical recalls Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handles with potential illumination failure. Affected units sold July-2020 to Dec-2020. No remedy specified in recall notice.
Laryngoscope handles may not illuminate as intended.
Flexicare Medical is recalling Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handles that may not illuminate properly. This could affect medical procedures requiring clear visualization. The recall covers specific production lots sold between July and December 2020.
The handles may not illuminate as intended, which could lead to poor visibility during medical procedures. This might cause errors in diagnosis or treatment. The hazard is specific to the illumination function of the laryngoscope handle.
Healthcare professionals using the Britepro Solo Stubby handles for medical procedures are most at risk. Patients undergoing procedures with these handles could experience inadequate visualization.
Check for the model reference REF:040-03-0000U on the handle. Affected units were produced from 2007xxxxx to 2012xxxxx and sold between July and December 2020.
Look for the model reference REF:040-03-0000U on the handle to confirm if it's affected.
The recall notice does not specify any remedy.
The recall notice does not provide specific action steps for affected users.
These handles were sold between July and December 2020.
We’ve drafted a message you can send Flexicare Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2185-2025 — Flexicare Medical Flexicare Medical Hello, I own a Flexicare Medical that is covered by recall Z-2185-2025 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.