Flexicare Medical recalls BritePro Solo Single-Use Fiber Optic Laryngoscope Handles and Blades with model numbers 040-331U to 040-362U sold between July 2020 and December 2020. Handles may not illuminate as intended.
Laryngoscope handles may not illuminate as intended.
Flexicare Medical is recalling BritePro Solo Single-Use Fiber Optic Laryngoscope Handles and Blades with specific model numbers and production dates. The handles may not illuminate as intended, which could affect medical procedures.
The handles may not illuminate properly during medical procedures. This could lead to difficulties in visualizing the airway, potentially affecting the safety of the procedure.
Medical professionals using these laryngoscope handles and blades for procedures. Patients and staff at facilities using the recalled models are most at risk.
Check for model numbers 040-331U (Mac 1) through 040-362U (Phillips 2) on the product. These were sold between July 2020 and December 2020.
Identify the model number on the handle or blade to confirm if it is in the recalled range.
Model numbers 040-331U (Mac 1) through 040-362U (Phillips 2).
Sold between July 2020 and December 2020.
The recall does not specify a stop-use instruction, so you can continue using them if they function properly.
We’ve drafted a message you can send Flexicare Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2183-2025 — Flexicare Medical Flexicare Medical Hello, I own a Flexicare Medical that is covered by recall Z-2183-2025 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.
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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.
