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

Recall Z-1681-2025 — CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, CE ENGLISH 1/EA, Model Number: 21-2111-0402-51; 2) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, YELLOW, CE ENGLISH 1/EA, Model Number: 21-2112-0402-51; 3) PUMP KIT, CADD-SOLIS, YELLOW, MODEL 2110 1/EA, Model N

U.S. FDA — Device Enforcement · United States · 2025-04-10 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1681-2025
Date of alert
2025-04-10
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Smiths Medical ASD, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15019517154290
Reported risk: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
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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