---
title: "Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusabl... — FDA record Z-0332-2022 | Is It on Recall"
description: "Intermittent risk of electric shock to users if an affected charger is used in conjunction with a faulty or bypassed institutions Mains Protective Earth (Ground"
url: https://isitonrecall.com/recall/fda-device-z-0332-2022-covidien-sonicision-battery-charger-intended-to-charge-the-sonicision-reusable-battery-pack-and-to-p/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide informatio... — FDA record Z-0332-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 12, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA
- **Reason**: Intermittent risk of electric shock to users if an affected charger is used in conjunction with a faulty or bypassed institutions Mains Protective Earth (Ground) circuit
- **Classification**: Class II
- **Recalling firm**: Covidien Llc
- **Quantity**: 2 units OUS
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0332-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0332-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Serial Numbers: MCSB006939, MCSB006947 GTIN: 10884521592896 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Brazil

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Dec 15, 2021
- **Recall initiation date**: Nov 12, 2021
- **Center classification date**: Dec 3, 2021

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0332-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Covidien Llc records](https://isitonrecall.com/brand/covidien-llc/)