Recall archive / 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. Source coverage and dates.
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
What the recall classes mean. 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.