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

Recall Z-0466-2025 — smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis infusion pumps

U.S. FDA — Device Enforcement · United States · 2024-06-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0466-2025
Date of alert
2024-06-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smiths Medical ASD, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15019517126844
Reported risk: The adapter input plug can become damaged or broken. If the input plug is damaged, the metal contacts to the body of the AC adapter may be exposed or one or more of the AC mains prongs may separate from the input plug.
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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