Trifurcated Extension Set — Class II medical device recall Z-0931-2014
Terminated recall by CareFusion 303, Inc., reported 2014-02-12, distributed nationwide. CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a def
| Recall number | Z-0931-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2014-01-16 |
| Classified | 2014-02-04 |
| Reported by FDA | 2014-02-12 |
| Terminated | 2014-08-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 9,550 units |
| Reason classes | packaging |
| Lot numbers | 11066540, 11075718, 11085047, 11086237, 11086676, 11095178, 11096312, 11106045, 11126756, 12025801, 12037064, 12037127, 12065225, 12065586, 12076327, 12095460, 13015666, 13025322, 13035514, 13076233, 13085002 |
| Model numbers | 1224, 9230 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0931-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.