Medline recalls newborn resuscitation kits and medical drawers with faulty laryngoscope handles that don't illuminate properly. Affected kits have specific kit numbers and lot numbers.
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 newborn resuscitation kits and medical drawers that contain laryngoscope handles which fail to illuminate properly. This could lead to inadequate visualization during critical medical procedures.
The laryngoscope handles in these kits have a failure to illuminate as intended. This means healthcare workers may not see the airway properly during critical newborn resuscitation procedures, potentially leading to ineffective treatment.
Healthcare providers using Medline newborn resuscitation kits or medical drawers with the specified kit numbers are most at risk. These kits are used in hospitals and clinics for emergency infant care.
Check if your kit has the following numbers: ACC010381C, ACC010532, ACC010671, or ACC010728. The specific lot numbers and UDI/DI codes are listed in the recall notice.
Identify if your kit has the specific numbers ACC010381C, ACC010532, ACC010671, or ACC010728.
Reach out to Medline Industries for guidance on next steps if you have the affected kit numbers.
The laryngoscope handles in these kits fail to illuminate properly, which could lead to inadequate visualization during critical newborn resuscitation procedures.
Check if your kit has the specific numbers ACC010381C, ACC010532, ACC010671, or ACC010728. Contact Medline for further instructions.
Yes, the failure to illuminate could lead to ineffective treatment during critical newborn resuscitation procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2567-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2567-2025 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.
