Plum A+ Infusion Pump — Class II medical device recall Z-0207-2014
Terminated recall by Hospira Inc., reported 2013-11-20, distributed nationwide. Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. The following er
| Recall number | Z-0207-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2012-02-05 |
| Classified | 2013-11-14 |
| Reported by FDA | 2013-11-20 |
| Terminated | 2016-11-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | DO, HR |
| Reason classes | device malfunction |
| Serial numbers | 13840001, 13840002, 13840003, 13840004, 13840005, 13840006, 13840007, 13840008, 13840009, 13840010, 13840011, 13840012, 13840013, 13840014, 13840015, 13840016, 13840017, 13840018, 13840019, 13840020, 13840021, 13840022, 13840023, 13840024, 13840025 and 475 more |
Product
Plum A+ Infusion Pump; List Number: 12391; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
Reason for recall
Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. The following error codes may be displayed during setup or infusion signifying possible calibration drift: E180/N180, E181/N181, E186/N186, E187/N187 or E346. Additionally, if the pressure sensor calibration has drifted, users may experience false distal occlusion alarms or distal occlusions that may not
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-0207-2014. 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.