Skip to content
Recall Observatory FDA recall evidence

Device product

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

Z-0931-2014

January 16, 2014

Class II

Product summary

Firm
CareFusion 303, Inc.
Event
Event 67326
Status
Terminated
Classification
Class II
Quantity
9,550 units
Official record key
device-enforcement:Z-0931-2014

Official wording

Reason: 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.

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.