CareFusion 303, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0931-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 16, 2014

Date Posted: February 12, 2014

Recall Number: Z-0931-2014

Event ID: 67326

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.

Status: Terminated

Product Quantity: 9,550 units

Code Information:

Trifurcated Extension Set, Model No. ME 1224, Lot No. 11066540 11075718 11085047 11086237 11086676 11095178 11096312 11106045 11126756 12025801 12037064 12037127 12065225 12065586 12076327 12095460 13025322 13035514 13076233 13085002 Trifurcated Extension Set, Model No. MP 9230 Lot No. 13015666.

Distribution Pattern:

Nationwide in US and Canada

Voluntary or Mandated:

Voluntary: Firm initiated