# FDA recall Z-0305-2021

> **CME America LLC** · Class II · device recall initiated 2020-02-27.

## Product

CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X L0/$$72019-0364/ 16D20191101/*    Lot Number Label: BODYGUARD LOT 2019-0364 Manufacturing Date: 2019 - 11-01 , LABEL I.D. SM-0642 REV. 01,   CMEAmerica  Wall Charger Kit, REF 151-143XLP, Contents; Wall Charger, Instructions, +B101150143XLP0/$$7A23456/16D000112010, Manufactured By: CME America LLC, 14988 W. 6th Ave., Suite 830, Golden. CO 80401, USA,   SM-0706 Rev 00    External Charger INPUT ; AC 100-240V, 50-60Hz; 10W, 0.3A max., OUTPUT: DC 8.4V, 300mA/DC 9V, 800mA, CME America, LLC , Label ID: SM-0718, Rev. 00    Label, Wall Mount Charger, Pump Service: Use with CME Pumps & Accessories ONLY. Refer Servicing to Qualified Personnel., LABEL I.D. : SM-0756 REV 00

## Reason for recall

The wall charger may not properly charge the infusion pump battery.

## Distribution

U.S. Consignees: 3, IL, MO, KS   OUS : 0 "No foreign consignees".

## Key facts

- **Recall number:** Z-0305-2021
- **Recalling firm:** CME America LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-27
- **Report date:** 2020-11-04
- **Termination date:** 2022-01-26

- **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-0305-2021

## Citation

> AI Analytics. FDA recall Z-0305-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0305-2021. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*