LifeCare 5000 Pump — Class II medical device recall Z-1702-2014
Terminated recall by Hospira Inc., reported 2014-06-11, distributed nationwide. There is the potential for the door roller assembly on the Plum LifeCare 5000 Series and Plum XL families of i
| Recall number | Z-1702-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2014-01-24 |
| Classified | 2014-06-03 |
| Reported by FDA | 2014-06-11 |
| Terminated | 2016-11-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AU, BE, BG, BH, BR, CA, CH, CL, CO, CZ, DE, EG, ES, FI, FR, GB, GR, HK, HR, HU, IL, IT, JO, KW, LU, MX, OM, PE, PL, PT, QA, RU, SA, SE, TR, TW, ZA |
| Reason classes | device malfunction |
Product
LifeCare 5000 Pump (Plum 1.6) infusion pump, indicated for volumetric infusion of critical drugs and fluids by intravenous (I.V.) administration.
Reason for recall
There is the potential for the door roller assembly on the Plum LifeCare 5000 Series and Plum XL families of infusers to break. In the event of a broken door roller pin, the door cannot appropriately lock the cassette in the right position. Depending on the conditions of a broken door roller pin, a number of events can occur. The door cannot be closed or a cassette/door alarm or a false occlusion
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-1702-2014. 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.