Plum A+3 Infusion Pump — Class II medical device recall Z-2725-2016
Terminated recall by Hospira Inc., reported 2016-09-14, distributed nationwide. The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and del
| Recall number | Z-2725-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2013-02-06 |
| Classified | 2016-09-06 |
| Reported by FDA | 2016-09-14 |
| Terminated | 2016-11-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | CR, DO |
| Quantity | 357,778 total |
| 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+3 Infusion Pump. List Number 12391. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor based infusion devices.
Reason for recall
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
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-2725-2016. 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.