Reported Mar 23, 2016 · Terminated
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
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 VersaSafe Infusion Set, Model No. 2122-0007
- Lot codes and dates
- Lot No. 13085603
- Amount recalled
- 5,760 units
Where it was sold
Why it was recalled
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
This product could cause temporary or reversible health problems — stop using it.
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