Medline recalls specific intubation trays due to light failure in Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. Affected kits include adult intubation trays with kit numbers ACC010369B through DYNJAA245A.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.
Medline is recalling 12 specific medical intubation trays because the light in the Flexicare BritePro Solo Fiber Optic Laryngoscope Handles fails to illuminate properly. This could lead to improper airway management during medical procedures.
The Flexicare BritePro Solo Fiber Optic Laryngoscope Handles in these kits do not illuminate the airway properly, which can cause improper intubation. This risk is present during medical procedures where clear visualization of the airway is critical.
Healthcare professionals using the recalled intubation trays for medical procedures are most at risk. Patients undergoing intubation may be affected if the light fails to illuminate.
Check for kit numbers ACC010369B through DYNJAA245A on Medline medical convenience kits. The affected items were sold with specific lot numbers and UDI/DI codes listed in the recall notice.
Identify if your intubation tray has kit numbers ACC010369B through DYNJAA245A as listed in the recall.
Reach out to Medline Industries for assistance with the recall process or to confirm if your item is affected.
The Flexicare BritePro Solo Fiber Optic Laryngoscope Handles in these kits fail to illuminate the airway properly, which can lead to improper intubation during medical procedures.
Check your kit number against the list provided in the recall notice. Contact Medline Industries for further assistance.
Yes, the failure to illuminate the airway can cause improper intubation, which may lead to complications during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2566-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2566-2025 from Medline. 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.
