Reported Aug 14, 2024 · Ongoing
CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-2120 , 21-2125 , and 21-2127 ) Indicated for the following…
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 PumpsModel 2120 ( 21-212021-2125and 21-2127 )
- Indicated for the following usesIntra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses
- Lot codes and dates
REF List Number 21-2120-0100-02UDI/DI 10610586040429
- Serial Numbers
1033919REF List Number 21-2120-0100-03UDI/DI 30610586040430
- Serial Numbers
10243071024333102529910278691027794REF List Number 21-2120-0100-50UDI/DI 10610586038501
- Serial Numbers
74 of 74 codes
101510410326371019622101966610196771019718101972010197901019795101980610198121019907102097810209841021003102114610211601021161102122910212371021271102128510115941011601101161610116181011638101164010127151012721101272610127361021319102138210213931023095102645510266621026793102776010310231031026103169610323601032375103237710323811032556103256010325681032569103257010325781032607103263310343671034394103441110344121034424
- Serial Numbers
107458011000011099307109941910994211099440REF List Number 21-2120-0102-03UDI/DI 10610586042607
- Serial Numbers
10426691055355107136010742871076699107968810896831054757109249910925371092547109256110925701094041109482410996891099700109971210997161099727109973211008451101619110293011029321103442110761511076561108010110801611083881113382111341111174181117437112153710948491108405REF List Number 21-2120-0102-06UDI/DI 10610586042614
- Serial Numbers
103763810464631046464110896511089831130680REF List Number 21-2120-0102-51UDI/DI 10610586042829
- Serial Numbers
1,733 of 1,733 codes
105893910409051068036106600211144661077271104098210773731077404107761010776191078365107840610786971078714107872511080971085482109313510854851093180112182411074901040654107885410965291034466103447510344781034482103448310344861034488103452210345281034533103453710345381034540103454510345461034561103456510345691034580103458610345931034595103459610345981034681103474810347521034784103484010348521034857103485810348591034868
- Serial Numbers
1,698 of 1,698 codes
11168810035541007973100871511006471118647101020010118451011990101372010591991104858103482710797551081617108391310893221089384110523410172541017504110126511012831106364104152011009821095965110780810503571051518105153210515341118637102550910344611034467103446910345291034549103455010345541034555103455710345581034564103457610345791034584103463810346911034747103474910347501034780103482610348281034838103483910348411034842
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Why it was recalled
Stop using this product now
The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidural space, or subarachnoid space infusion.
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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