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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Medline Industries, LP
- Product type
- Intubation Tray
- Model numbers
- Kit lots 25IBC172 25HBJ413 UDI (ea) 10198459480317 UDI (case) 40198459480318
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 24, 2025
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
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
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
- Locate the SKU on the product packaging
- Verify if it matches DYNJAA245B
- 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.
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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
- Risk of hypoxia and respiratory failure
- Stop using the product immediately
- Contact Medline for further instructions
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Safety Guide
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