Medline Industries, LP: Medical Device Recall in 2026 - (Recall #: Z-1312-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 24, 2025

Date Posted: February 18, 2026

Recall Number: Z-1312-2026

Event ID: 98285

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 141,971

Code Information:

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

Distribution Pattern:

Distribution US nationwide and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated