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.
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.
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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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.
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.
This recall is not part of a broader industry pattern.
The recall may cause delays in emergency procedures, leading to significant health risks for patients requiring intubation.
The SKU and model numbers can typically be found on the box or packaging of the Intubation Tray.
Expect a refund or replacement within 4-6 weeks after returning the product.
Keep records of your purchase, any communications with the manufacturer, and document any incidents related to the product.
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.
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