FDAClass IIFebruary 18, 2026

Medline 14 Fr Suction Catheter Kits recall

Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit

Why was Medline 14 Fr Suction Catheter Kits recalled?

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 should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Kit lot 48625040001 UDI (ea) 10080196033317 UDI (case) 40080196033318¿

Product
Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
Recalling firm
Medline Industries, LP
Quantity
141,971
Distribution
Distribution US nationwide and Canada.
Recall date
February 18, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls