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Use caution Medical device recall · FDA · Published July 25, 2025

Medline medical kits recalled: Light failure in intubation trays

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2566-2025Medical deviceMedline ›
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Contact the company

Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/51736-medline-medical-kits-recalled-light-failure-in-intubation-trays.

Source Summary by GovInfoNow · govinfonow.com/recall/51736-medline-medical-kits-recalled-light-failure-in-intubation-trays · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2566-2025

Cite this page

“Medline medical kits recalled: Light failure in intubation trays.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51736-medline-medical-kits-recalled-light-failure-in-intubation-trays. Based on FDA recall #Z-2566-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2566-2025%22&limit=1).

The FDA announced on July 25, 2025, that Medline Industries LP recalled specific Medline medical convenience kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles because the light may fail to illuminate. The agency issued recall number Z-2566-2025 for the Class I voluntary recall.

How to tell if you have it

  • Brand: Medline
  • Kit Number ACC010369B, UDI/DI 10193489777512 (EA) 40193489777513(CA)
  • Kit Number ACC010379A, UDI/DI 10193489777529 (EA) 40193489777520(CA)
  • Kit Number ACC010392, UDI/DI 10193489218053 (EA) 40193489218054(CA)
  • Kit Number ACC010467A, UDI/DI 10193489834550 (EA) 40193489834551(CA)
  • Kit Number ACC010469, UDI/DI 10193489414677 (EA) 40193489414678(CA)
  • Kit Number ACC010480, UDI/DI 10193489499933 (EA) 40193489499934(CA)
  • Kit Number ACC010480A, UDI/DI 10195327009366 (EA) 40195327009367(CA)
  • Kit Number ACC010540, UDI/DI 10193489977547 (EA) 40193489977548(CA)
  • Kit Number ACC010593A, UDI/DI 10195327168995 (EA) 40195327168996(CA)
  • Kit Number ACC010593B, UDI/DI 10195327195472 (EA) 40195327195473(CA)
  • Kit Number DYNDA1847A, UDI/DI 10193489481259 (EA) 40193489481250(CA)
  • Kit Number DYNJAA245A, UDI/DI 10193489804584 (EA) 40193489804585(CA)

The hazard

The recalled kits contain Flexicare BritePro Solo Fiber Optic Laryngoscope Handles that may fail to illuminate as intended. The FDA classified this defect as a Class I recall, indicating a high risk of serious adverse health consequences or death.

Context

GovInfoNow's records show Medline Industries LP has issued 119 other recalls since October 22, 2021. On July 23, 2025, the company recalled Foley Tray Kits due to incorrect labeling risk involving SureStep systems. Other recent recalls of similar products include Medline Intubation Tray Recall: Risk of Airway Obstruction from Wrong Suction Catheter (December 24, 2025) and Medline Convenience Kits Recall: Quality Issues With Anesthesia Sets (May 6, 2026).

How to tell if you have this one

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.

  • Brand
    Medline
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Ongoing
  • Distribution
    US distribution to: AL, CA, DE, OR, TN, TX
Recall numberProduct, codes & lotsQuantity
Z-2566-2025Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A; 3. INTUBATION TRAY, Kit Number ACC010392; 4. INTUBATION KIT, Kit Number ACC010467A; 5. ADULT AIRWAY TRAY, Kit Number ACC010469; 6. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480; 7. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480A; 8. ADULT INTUBATION, Kit Number ACC010540; 9. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593A; 10. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593B; 11. INTUBATION TRAY, Kit Number DYNDA1847A; 12. INTUBATION TRAY (ADULT), Kit Number DYNJAA245A.; 1. ACC010369B, UDI/DI 10193489777512 (EA) 40193489777513(CA), Lot Numbers: 2. ACC010379A; 10193489777529 (EA) 40193489777520(CA), Lot Numbers: 3. ACC010392; 10193489218053 (EA) 40193489218054(CA), Lot Numbers: 4. ACC010467A; 10193489834550 (EA) 40193489834551(CA), Lot Numbers: 5. ACC010469; 10193489414677 (EA) 40193489414678(CA), Lot Numbers: 6. ACC010480; 10193489499933 (EA) 40193489499934(CA), Lot Numbers: 7. ACC010480A; 10195327009366 (EA) 40195327009367(CA), Lot Numbers: 8. ACC010540; 10193489977547 (EA) 40193489977548(CA), Lot Numbers: 9. ACC010593A; 10195327168995 (EA) 40195327168996(CA), Lot Numbers: 10. ACC010593B; 10195327195472 (EA) 40195327195473(CA), Lot Numbers: 11. DYNDA1847A; 10193489481259 (EA) 40193489481250(CA), Lot Numbers: 12. DYNJAA245A. 10193489804584 (EA) 40193489804585(CA), Lot Numbers:2520 units
Z-2567-2025Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITION 3, Kit Number ACC010532; 3. DRAWER #4C ADULT, Kit Number ACC010671; 4. DRAWER #2, Kit Number ACC010728.; 1. ACC010381C: UDI/DI 10193489922127 (EA), 40193489922128 (CS), Kit Lot Numbers: 2. ACC010532: UDI/DI 10193489902358 (EA), 40193489902359 (CS), Kit Lot Numbers: 3. ACC010671: UDI/DI 10195327351090 (EA), 40195327351091 (CS), Kit Lot Numbers: 4. ACC010728: UDI/DI 10195327506544 (EA), 40195327506545 (CS), Kit Lot Numbers:596 units
Based on the official FDA remedy

What to do — step by step

  1. Check Kit Numbers

    Identify if your intubation tray has kit numbers ACC010369B through DYNJAA245A as listed in the recall.

  2. Contact Medline

    Reach out to Medline Industries for assistance with the recall process or to confirm if your item is affected.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: yesDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: yesALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “US distribution to: AL, CA, DE, OR, TN, TX” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, California, Delaware, Oregon, Tennessee, Texas.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Jul 25, 202512. FDA classified it Class I: Sep 19, 202523. Published in FDA’s Enforcement Report: Oct 1, 202532025
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-2566-2025 (July 25, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2566-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA