Plum 360 Infusion Pump — Class II medical device recall Z-1682-2017
Terminated recall by Hospira Inc., A Pfizer Company, reported 2017-04-05, distributed nationwide. Depleted Battery alarm shows instead of Replace Battery. On battery power, ongoing therapy stops, alarms show
| Recall number | Z-1682-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., A Pfizer Company, Lake Forest, IL, United States |
| Recall initiated | 2016-12-30 |
| Classified | 2017-03-24 |
| Reported by FDA | 2017-04-05 |
| Terminated | 2019-07-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, CL, ES, FR, GB, GR, HK, IE, IT, JO, KW, MX, NZ, OM, PH, PL, SA, TR |
| Quantity | 62,847 units |
| Serial numbers | 199, 19985403, 19985406, 19985408, 19985428, 19985439, 19985440, 19985450, 19985464, 19985878, 19985879, 19985880, 19985881, 19985882, 19985883, 19985884, 19985885, 19985886, 19985887, 19985889, 19985890, 19985891, 19985892, 19985893, 19985894 and 475 more |
Product
Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions
Reason for recall
Depleted Battery alarm shows instead of Replace Battery. On battery power, ongoing therapy stops, alarms show and sound, pump shuts down after 3 minutes. On AC power, the pump reboots (takes about 25 seconds). Therapy can resume. AC power interruption of 3-7 seconds prompts an incorrect E323 alarm, ongoing therapy stop, and pump reboot. Longer power loss results in battery power operation.
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-1682-2017. 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.