Reported Nov 4, 2020 · Terminated

CMEAmerica BodyGuard Wall Charger

CME America LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: CME America LLC · 14998 W 6th Ave Ste 830 · Golden, CO · 80401-5025

Is this the product you have?

CMEAmerica BodyGuard Wall Charger

4 of 4 products

Products covered by this recall
Model / numberProduct as published
151-143XLLot number 2019-0364, Mode/ , *+B 01151143X L0/$$72019-0364/ 16D20191101/*
Lot Number Label: BODYGUARD
LOT 2019-0364 Manufacturing Date: 2019 - 11-01 , LABEL I.D. SM-0642 REV. 01, CMEAmerica Wall Charger Kit
151-143XLPContents; Wall Charger, Instructions, +B101150143XLP0/$$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
Lot codes and dates
  • Catalog NO. 151-143XL LOT NO. 2019-0364
Amount recalled
27 chargers

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 26, 2022 · Data as of Sep 19, 5:44 PM UTC

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