CADD-Solis Battery Pack (Smiths Medical) – Adapter Damage Risk (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Smiths Medical ASD, Inc.
Lot Codes / Batch Numbers
Model 21-0270-25, UDI/DI 15019517126844, All lots
Products Sold
Model 21-0270-25, UDI/DI 15019517126844, All lots
Smiths Medical ASD, Inc. is recalling smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Smiths Medical issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 06/26/2024 via letter distributed by a traceable means. The notice explained the issue, potential risk, and requested the following: Locate all Model 21-0270-25 AC Adapters in your possession. Inspect the AC Adapter for damage to the input plug, missing AC prongs, or exposed metal contacts. If damaged, remove the AC Adapter from service and submit a request for credit to Smiths Medical at 800-258-5361. Distributors were directed to forward to the notice to those to whom the they distributed the device with the request to complete the response form and return it to smithsmedical8528@sedgwick.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026