The Metrix Company: Medical Device Recall in 2024 - (Recall #: Z-0343-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Imed Products Imed EVA BAG, 250 mL, 2-PORTS, REF IM68045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.

Product Classification:

Class II

Date Initiated: October 9, 2024

Date Posted: November 20, 2024

Recall Number: Z-0343-2025

Event ID: 95499

Reason for Recall:

A limited number of IV bags have been found to leak during filling.

Status: Ongoing

Product Quantity: 1056 cases of 50 units

Code Information:

UDI/DI 00812496011312, Lot Numbers: 68045-A8289, 68045-A8319, 68045-A8347, 68045-A8390, 68045-A8434

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of TX, IL, OH, PA, WA, MD, IL, UT, CA, MA, PA, MI, FL, PR, and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated