Reported Oct 27, 2021 · Terminated
CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d.…
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?
14 of 14 products
| # | Product as published |
|---|---|
| 1 | 21-2120-0105-02L |
| 2 | 21-2120-0105-03L |
| 3 | 21-2120-0105-06L |
| 4 | 21-2120-0105-07L |
| 5 | 21-2120-0105-08L |
| 6 | 21-2120-0105-12L |
| 7 | 21-2120-0105-13L |
| 8 | 21-2120-0105-14L |
| 9 | 21-2120-0105-15L |
| 10 | 21-2120-0105-17L |
| 11 | 21-2120-0105-50L |
| 12 | 21-2127-0105-02L |
| 13 | 21-2127-0105-06L |
| 14 | 21-2127-0105-50L |
- Lot codes and dates
- a. 21-2120-0105-02L
- Serial Numbers
273 of 273 codes
117150211715361171537117153811715391171540117154111715421171543117154411715451171546117154711715481171549117155011715511171552117155311715541171555117155611715571171558117155911715601171561117156211715631171564117156511715661171567117156811715691171570117157111715721171573117157411715751171576117157711715781171579117158011715811171582117158311715841171632117163311716491171650117166511716661171667117166811716691171670
- Serial Numbers
105 of 105 codes
117161611716181171619117162011716221171631117163411716351171636117165111716521171653117168411716851171686117168711716881171689117169011716911171692117169311783561178357117835811783591178360117836111783621178859117886011788621178863117886411788651178866117886711788681178869117887011788711178872117887311788741178875117887611788771178878117887911788801178881117888211788831178884117898111789821178983117898411789851178986
- Serial Numbers
71 of 71 codes
117140511714061171407117140811714091171410117141111714121171413117141411714151171416117141711714181171419117142011714211171422117142311714241171425117142611714271171428117142911714301171431117143211714331171434117143511714361171437117143811714391171440117144111714421171443117144411714451171446117144711714481171449117145011714511171452117145311714541171455117145611714571171458117145911714601171461117146211714631171464
- Serial Numbers
11716261171627117162811716291171630 e. 21-2120-0105-08L
- Serial Numbers
76 of 76 codes
117146911714701171471117147211714731171474117147511714761171477117147811714791171485117148611714871171488117148911714901171491117149211714931171494117149511714961171497117149811714991171500117150111715031171504117158511715861171587117158811715891171590117159111715921171593117159411715981171599117160011716011171602117160311716041171605117160611716071171608117160911716101171623117162411716251171643117164411716451171646
- Serial Numbers
11714801171481 g. 21-2120-0105-13L
- Serial Numbers
117161111716121171613117161411716151179158 h. 21-2120-0105-14L
- Serial Numbers
11783631178366117909611790971179132117913311791351179136117913711792171179242 i. 21-2120-0105-15L
- Serial Numbers
1171595117159611715971178887117888811788891178890117889111788931178894117889511788961178897117889811791031179105117910611791071179108117910911791101179112117911311791141179115117911611791171179118117911911791201179121117912211791231179124 j. 21-2120-0105-17L
- Serial Numbers
11715051171506117150711715081171509117151011715111171512117151311715141171526117152711715281171529117153011715311171532117153311715341171535117913811791391179140 k. 21-2120-0105-50L
- Serial Numbers
117151611715181171520117152411790981179099117910011791011179102 l. 21-2127-0105-02L
- Serial Numbers
117912511791271179128117912911792181179219117922011792221179223117922411792251179226117922811792301179232117923311792341179235117923611792371179238117923911792401179241 m. 21-2127-0105-06L
- Serial Numbers1171621 n. 21-2127-0105-50L
- Serial Numbers
11783541178355
- Amount recalled
- 642 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Stop using this product now
Specific Pumps may exhibit intermittent performance in the AILD (Air in Line Detector) function. If an AILD does not sufficiently discern fluid from air in line, an air in line event may not be recognized by the pump and may not alarm to notify the clinician.
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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