Medline Industries, LP: Medical Device Recall in 2026 - (Recall #: Z-1407-2026)

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 Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A

Product Classification:

Class II

Date Initiated: January 7, 2026

Date Posted: February 25, 2026

Recall Number: Z-1407-2026

Event ID: 98329

Reason for Recall:

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

Status: Ongoing

Product Quantity: 15 units

Code Information:

1) DYNDM1031A, UDI-DI: 10884389555897(each), 40884389555898(case), Lot Number: 23EBM150

Distribution Pattern:

Worldwide distribution - US Nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated