PlainRecalls
FDA Devices Moderate Class II Terminated

Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.

Reported: February 12, 2014 Initiated: January 16, 2014 #Z-0931-2014

Product Description

Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.

Reason for Recall

CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak.

Details

Recalling Firm
CareFusion 303, Inc.
Units Affected
9,550 units
Distribution
Nationwide in US and Canada
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.. Recalled by CareFusion 303, Inc.. Units affected: 9,550 units.
Why was this product recalled?
CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 12, 2014. Severity: Moderate. Recall number: Z-0931-2014.