Z-0466-2025 Class II Ongoing
FDA device recall Z-0466-2025 was initiated by Smiths Medical ASD, Inc. on Jun 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… The recall status is ongoing. Affected quantity: 156,400 AC adapters.
Recall Details
- Product Type
- Devices
- Report Date
- Nov 27, 2024
- Initiation Date
- Jun 26, 2024
- 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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0466-2025
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026