The Recall Desk
HighFDA (Devices)·Z-0305-2021·Announced 2020-11-04

CMEAmerica BodyGuard Wall Charger Recalled for Charging Defect

CME America LLC is recalling 27 BodyGuard Wall Chargers because they may not properly charge the infusion pump battery.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device (infusion pump charger) with a functional defect that could prevent proper battery charging, representing a risk of harm to patients relying on the device, although no specific injuries or illnesses are reported in the source text.

Plain-English summary

CME America LLC is recalling 27 units of the BodyGuard Wall Charger (Lot number 2019-0364, Mode/Catalogue number 151-143XL). The recall was initiated because the wall charger may not properly charge the infusion pump battery.

The affected chargers were distributed to three U.S. consignees located in Illinois, Missouri, and Kansas. No foreign consignees were involved in the distribution of this specific lot.

Consumers who possess this specific lot of the BodyGuard Wall Charger should stop using it and contact CME America LLC for instructions on how to proceed.

The recalled product

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 1
Manufacturer
CME America LLC
Category
Medical Device — Infusion Pump Accessories
Hazard
Affected units
27

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Catalog NO. 151-143XL LOT NO. 2019-0364

Distribution

Distributed in 3 states:

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Same hazard · charging defect

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