# FDA recall Z-0332-2022

> **Covidien Llc** · Class II · device recall initiated 2021-11-12.

## 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 for recall

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

## Distribution

Brazil

## Key facts

- **Recall number:** Z-0332-2022
- **Recalling firm:** Covidien Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-11-12
- **Report date:** 2021-12-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0332-2022

## Citation

> AI Analytics. FDA recall Z-0332-2022. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-0332-2022. Source: US FDA. Licensed CC0.

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