HIGH

Medline Recalls Intubation Tray Over High Hypoxia Risk

Medline Industries, LP recalled 130 Intubation Trays on December 24, 2025. The recalled trays may contain a smaller suction catheter that could cause respiratory failure. Patients and healthcare providers should stop using the device immediately.

Quick Facts at a Glance

Recall Date
December 24, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter

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About This Product

The Intubation Tray is used in medical settings for emergency airway management. Healthcare providers rely on the correct suction catheter size to ensure patient safety during intubation procedures.

Why This Is Dangerous

The potential for a smaller 8 Fr Suction Catheter to replace the required 14 Fr Suction Catheter can lead to inadequate airway management, resulting in severe respiratory complications.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall may cause delays in emergency procedures, leading to significant health risks for patients requiring intubation.

Practical Guidance

How to identify if yours is affected

  1. Locate the SKU on the product packaging
  2. Verify if it matches DYNJAA245B
  3. Check the model lots for 25IBC172 or 25HBJ413

Where to find product info

The SKU and model numbers can typically be found on the box or packaging of the Intubation Tray.

What timeline to expect

Expect a refund or replacement within 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Contact Medline Industries again
  • Reach out to consumer protection agencies
  • Document all communications for reference

How to prevent similar issues

  • Always verify the catheter size before use
  • Purchase medical devices from reputable suppliers
  • Stay informed about product recalls

Documentation advice

Keep records of your purchase, any communications with the manufacturer, and document any incidents related to the product.

Product Details

The recalled product is the Intubation Tray (Adult) containing Suction Catheter Kits, SKU DYNJAA245B. The affected model lots are 25IBC172 and 25HBJ413. The product was distributed nationwide in the U.S. and Canada.

Key Facts

  • 130 units recalled
  • Risk of hypoxia and respiratory failure
  • Stop using the product immediately
  • Contact Medline for further instructions
View Original Recall on FDA - Medical Devices

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Safety Guide

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeIntubation Tray
Sold At
Multiple Retailers

Product Details

Model Numbers
Kit lots 25IBC172 25HBJ413 UDI (ea) 10198459480317 UDI (case) 40198459480318
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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