# FDA recall Z-1886-2020

> **CME America, LLC** · Class II · device recall initiated 2020-01-14.

## Product

BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. (280 cm) - Blue Stripe - Product Usage: The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital and home care environments.

## Reason for recall

The filter installed onto the tube set may have the incorrect pore size.

## Distribution

US Nationwide distribution including in the states of AK, CA, IL, KS, MA, MO, and SD. No O.U.S.

## Key facts

- **Recall number:** Z-1886-2020
- **Recalling firm:** CME America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-01-14
- **Report date:** 2020-05-13
- **Termination date:** 2021-05-27

- **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-1886-2020

## Citation

> AI Analytics. FDA recall Z-1886-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1886-2020. Source: US FDA. Licensed CC0.

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