PlainRecalls
FDA Devices Moderate Class II Terminated

SmartSite Low Sorbing Infusion Set, Model# 10015048. Intravascular administration set.

Reported: October 2, 2013 Initiated: August 30, 2013 #Z-2285-2013

Product Description

SmartSite Low Sorbing Infusion Set, Model# 10015048. Intravascular administration set.

Reason for Recall

CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model# 10015048, because there is a potential for separation at the tubing sleeve below the drip chamber.

Details

Recalling Firm
CareFusion 303, Inc.
Units Affected
15860 units
Distribution
Nationwide in US: PA, OK, TX, FL, NC, CA, IN, WI
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
SmartSite Low Sorbing Infusion Set, Model# 10015048. Intravascular administration set.. Recalled by CareFusion 303, Inc.. Units affected: 15860 units.
Why was this product recalled?
CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model# 10015048, because there is a potential for separation at the tubing sleeve below the drip chamber.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 2, 2013. Severity: Moderate. Recall number: Z-2285-2013.