Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0332-2022 — 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

U.S. FDA — Device Enforcement · United States · 2021-11-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0332-2022
Date of alert
2021-11-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Covidien Llc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10884521592896
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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