Reported May 14, 2025 · Ongoing

CADD Solis VIP Ambulatory Infusion Pump Models

Smiths Medical ASD, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Smiths Medical ASD, Inc. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690

Is this the product you have?

CADD Solis VIP Ambulatory Infusion Pump Models

15 of 15 products

Products covered by this recall
Model / numberProduct as published
21-2127-0105-01PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE, 1/EA
21-2120-0105-01PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD ENABLED, 1/EA
21-2120-0103-01PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH 1/EA
21-2120-0102-51PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH 1/EA
21-2120-0104-01PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD ENABLED 1/EA
21-2120-0103-51PUMP KIT, CADD-SOLIS VIP, MDL 2120, CE GLOBAL ENGLISH 1/EA
21-2127-0104-01PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE 1/EA
21-2120-0105-00PUMP KIT, CADD-SOLIS VIP, MDL 2120, TRIAL/LOANER, NA ENGLISH, PHARMGUARD, 1/EA
21-2120-0103-78PUMP, CADD-SOLIS VIP, MDL 2120, TRIAL/LOANER CE GLOBAL ENGLISH 1/EA
21-2120-0102-78PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH, TRIAL/LOANER 1/EA
21-2120-0104-231PUMP, CADD-SOLIS VIP, MDL 2120, NFHU, NA ENGLISH, PHARMGUARD ENABLED 1/EA
21-2120-0102-249PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH, NFHU 1/EA
21-2120-0103-249PUMP, CADD-SOLIS VIP, MDL 2120, NFHU CE GLOBAL ENGLISH 1/EA
21-2125-0104-01PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, FACTORY LIBRARY 1/EA
21-2120-0102-249.PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH, NFHU 1/EA
Lot codes and dates
  • All serial numbers. 1 ) 21-2127-0105-01
  • UDI-DI
    • 15019517150292
    • 2 ) 21-2120-0105-01
  • UDI-DI
    • 15019517150001
    • 3 ) 21-2120-0103-01
  • UDI-DI
    • 15019517084368
    • 4 ) 21-2120-0102-51
  • UDI-DI
    • 10610586042829
    • 5 ) 21-2120-0104-01
  • UDI-DI
    • 15019517126587
    • 6 ) 21-2120-0103-51
  • UDI-DI
    • 15019517096378
    • 7 ) 21-2127-0104-01
  • UDI-DI
    • 15019517126600
    • 8 ) 21-2120-0105-00
  • UDI-DI
    • 15019517149999
    • 9 ) 21-2120-0103-78
  • UDI-DI
    • 15019517096392
    • 10 ) 21-2120-0102-78
  • UDI-DI
    • 10610586042836
    • 11 ) 21-2120-0104-231
  • UDI-DI
    • 15019517126617
    • 12 ) 21-2120-0102-249
  • UDI-DI
    • 10610586042843
    • 13 ) 21-2120-0103-249
  • UDI-DI
    • 15019517096385
    • 14 ) 21-2125-0104-01
  • UDI-DI
    • 15019517126594
    • 15 ) 21-2120-0102-249
  • UDI-DI10610586042843
Amount recalled
313,676 items

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:52 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.