Covidien Sonicision Battery Charger-intended to charge the Sonicision… — Class II medical device recall Z-0332-2022
Ongoing recall by Covidien Llc, reported 2021-12-15. Intermittent risk of electric shock to users if an affected charger is used in conjunction with a faulty or by
| Recall number | Z-0332-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien Llc, Mansfield, MA, United States |
| Recall initiated | 2021-11-12 |
| Classified | 2021-12-03 |
| Reported by FDA | 2021-12-15 |
| Countries outside the US | BR |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 10884521592896 |
| Serial numbers | MCSB006939, MCSB006947 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0332-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.