# FDA recall Z-1442-2020

> **CME America, LLC** · Class I · device recall initiated 2019-09-16.

## Product

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.

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-1442-2020
- **Recalling firm:** CME America, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-09-16
- **Report date:** 2020-03-18
- **Termination date:** 2022-04-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Golden, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1442-2020

## Citation

> AI Analytics. FDA recall Z-1442-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1442-2020. Source: US FDA. Licensed CC0.

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