The Metrix Company: Medical Device Recall in 2017 - (Recall #: Z-3240-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,

Product Classification:

Class II

Date Initiated: September 13, 2017

Date Posted: October 11, 2017

Recall Number: Z-3240-2017

Event ID: 78117

Reason for Recall:

The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as ordered and as labeled on the inner and outer boxes.

Status: Terminated

Product Quantity: 50 cases of 200 units

Code Information:

UDI: 50812496011850, Lot Numbers: 28990, 29093, 29135, 29244,

Distribution Pattern:

AZ, MA, IL, FL

Voluntary or Mandated:

Voluntary: Firm initiated