Reported May 14, 2025 · Ongoing

CADD-Solis VIP Ambulatory Infusion Pump; Model/Number: 21-2120-0100-02 21-2120-0100-03 21-2120-0100-06 21-2120-0100-232…

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
  • Model/Number

    69 of 69 codes

    • 21-2120-0100-02
    • 21-2120-0100-03
    • 21-2120-0100-06
    • 21-2120-0100-232
    • 21-2120-0100-233
    • 21-2120-0100-50
    • 21-2120-0100-51
    • 21-2120-0100-95
    • 21-2120-0102-02
    • 21-2120-0102-03
    • 21-2120-0102-06
    • 21-2120-0102-07
    • 21-2120-0102-08
    • 21-2120-0102-12
    • 21-2120-0102-13
    • 21-2120-0102-14
    • 21-2120-0102-15
    • 21-2120-0102-17
    • 21-2120-0102-237
    • 21-2120-0102-238
    • 21-2120-0102-247
    • 21-2120-0102-249
    • 21-2120-0102-51
    • 21-2120-0102-78
    • 21-2120-0102-92
    • 21-2120-0102-97
    • 21-2120-0102-98
    • 21-2120-0103-01
    • 21-2120-0103-02
    • 21-2120-0103-03
    • 21-2120-0103-06
    • 21-2120-0103-07
    • 21-2120-0103-08
    • 21-2120-0103-12
    • 21-2120-0103-14
    • 21-2120-0103-15
    • 21-2120-0103-17
    • 21-2120-0103-249
    • 21-2120-0103-51
    • 21-2120-0103-78
    • 21-2120-0104-01
    • 21-2120-0104-231
    • 21-2120-0105-00
    • 21-2120-0105-01
    • 21-2120-0105-02L
    • 21-2120-0105-03L
    • 21-2120-0105-06L
    • 21-2120-0105-07L
    • 21-2120-0105-08
    • 21-2120-0105-08L
    • 21-2120-0105-12L
    • 21-2120-0105-13L
    • 21-2120-0105-14L
    • 21-2120-0105-15L
    • 21-2120-0105-17L
    • 21-2120-0105-50
    • 21-2120-0105-50L
    • 21-2125-0104-01
    • 21-2125-0105-03L
    • 21-2125-0105-07L
Lot codes and dates
  • All CADD-Solis and CADD-Solis
  • VIP Ambulatory Infusion Pumps UDI-DI

    142 of 142 codes

    • 10610586034787
    • 10610586038778
    • 10610586038785
    • 10610586038808
    • 10610586038822
    • 10610586039232
    • 10610586041037
    • 10610586041051
    • 10610586042591
    • 10610586042669
    • 10610586042829
    • 10610586042836
    • 15019517084368
    • 15019517096378
    • 15019517096385
    • 15019517096392
    • 15019517099690
    • 15019517101003
    • 15019517101010
    • 15019517101034
    • 15019517101041
    • 15019517126587
    • 15019517126594
    • 15019517126600
    • 15019517126617
    • 15019517128697
    • 15019517135343
    • 15019517149999
    • 15019517150001
    • 15019517150292
    • 15019517154290
    • 15019517154887
    • 15019517154924
    • 15019517154979
    • 15019517154986
    • 15019517154993
    • 15019517155006
    • 15019517155013
    • 15019517155044
    • 15019517246735
    • 15019517247008
    • 15019517247169
    • 15019517247176
    • 15019517247183
    • 15019517247206
    • 00610586038900
    • 00610586039310
    • 04546027095620
    • 04546027095637
    • 04546027095644
    • 04546027095668
    • 04546027095675
    • 04546027095682
    • 04546027095699
    • 04546027095705
    • 04546027095712
    • 04546027095729
    • 04546027095736
    • 04546027095743
    • 04546027095897
    15019517150124¿
    • 15019517150131
    • 15019517150179
    • 15019517150193
    • 15019517150216
    • 15019517150278
    • 15019517150308
    • 15019517150315
    • 15019517150322
    • 15019517150391
    • 30610586035344
    • 30610586035368
    • 30610586035511
    • 30610586039205
    • 30610586039397
    • 30610586040430
    • 30610586040539
    • 35019517128677
    • 35019517128684
    • 35019517128691
    • 35019517128721
    • 35019517128738
    • 35019517128745
    • 35019517128769
    • 35019517128783
    • 35019517128837
    • 35019517135316
    • 35019517135323
    • 35019517135330
    • 35019517135354
    • 35019517135361
    • 35019517154850
    • 35019517154867
    • 35019517154874
    • 35019517154904
    • 35019517154911
    • 35019517154942
    • 35019517154959
    • 35019517154966
    • 35019517155031
    • 35019517155055
    • 35019517155062
    • 35019517155079
    • 35019517155086
    • 35019517155130
Amount recalled
185,975 US; 127,701 OUS Total

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

Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.

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, 4:55 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.