Z-0466-2025 Class II Ongoing

Recalled by Smiths Medical ASD, Inc. — Minneapolis, MN

FDA device recall Z-0466-2025 was initiated by Smiths Medical ASD, Inc. on June 26, 2024 and is designated Class II. Reason for recall: 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 f… The recall status is ongoing. Affected quantity: 156,400 AC adapters.

Recall Details

Product Type
Devices
Report Date
November 27, 2024
Initiation Date
June 26, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
156,400 AC adapters

Product Description

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

Reason for Recall

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.

Distribution Pattern

Worldwide distribution.

Code Information

Model 21-0270-25, UDI/DI 15019517126844, All lots