CME America, LLC: Medical Device Recall in 2020 - (Recall #: Z-1442-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The BodyGuard Infusion Pump System is designed to transfer medication and fluids intravenously.

Product Classification:

Class I

Date Initiated: September 16, 2019

Date Posted: March 18, 2020

Recall Number: Z-1442-2020

Event ID: 84985

Reason for Recall:

When using a specific tubing set with infusion pump system, may result in under deliver of fluids.

Status: Terminated

Product Quantity: 69400 infusion sets

Code Information:

Catalog Number: A120-003XYVA UDI: 00818666020146 Lot Numbers: 10636 10653 12117 12836 13156 13279 13656 13978 14057 14188 14545 14790 14966 15073 19486 19490 19492 19834 16173 14966 15073 15277 15434 15802

Distribution Pattern:

US: CA, OH, PA, and TX OUS: Canada

Voluntary or Mandated:

Voluntary: Firm initiated