The Metrix Company: Medical Device Recall in 2019 - (Recall #: Z-0005-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 3000mL, REF 66631 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.

Product Classification:

Class II

Date Initiated: September 21, 2018

Date Posted: October 9, 2019

Recall Number: Z-0005-2020

Event ID: 83509

Reason for Recall:

Potential for leaking product

Status: Ongoing

Product Quantity: 234720 bags

Code Information:

Lot Numbers: 66631-A2443, 66631-A2564, 66631-A2629, 66631-A2772, 66631-A2975, 66631-A3004, 66631-A3311, 66631-A3456, 66631-A3483, 66631-A3553, 66631-A3558, 66631-A3738, 66631-A3774, 66631-A3795, 66631-A3978, 66631-A4082, 66631-A4148, 66631-A4444, 66631-A4517, 66631-A5065, 66631-A5282, 66631-A5411, 66631-A5555, 66631-A5670

Distribution Pattern:

US Nationwide distribution including the states of PA, MA, IL CA.

Voluntary or Mandated:

Voluntary: Firm initiated