Reported Dec 30, 2015 · Terminated
Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or…
CareFusion 303, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
- Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
- Lot codes and dates
68 of 68 codes
150867331508693715095168150953321509577215096137150965161508675615095022150952121509533315095773150961831509662715086832150950451509521315095334150958421509618415096628150868331509508815095214150953471509584315096222150966291508686415095103150952541509549015095844150962911509670315086865150951281509525515095504150959361509629215096704150869101509513615095274150955051509602015096412150967221508691115095137150952751509556115096021150964131509672315086912150951661509528915095644
- Amount recalled
- 1,445,180 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set because the disconnection and leakage may occur during infusion.
This product could cause temporary or reversible health problems — stop using it.
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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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