The Plum A+ Infusion Systems are a multipurpose family of devices… — Class II medical device recall Z-2676-2017
Terminated recall by ICU, reported 2017-07-19, distributed nationwide. A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by
| Recall number | Z-2676-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ICU, Lake Forest, IL, United States |
| Recall initiated | 2013-02-01 |
| Classified | 2017-07-10 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2018-05-31 |
| Distributed | Nationwide (US) |
| Quantity | 10,609 units |
| Serial numbers | 131, 13120009, 13120017, 13120018, 13120019, 13120026, 13120028, 13120037, 13120041, 13120042, 13120044, 13120057, 13120058, 13120068, 13120071, 13120074, 13120075, 13120082, 13120096, 13120103, 13120104, 13120107, 13120108, 13120109, 13120115 and 475 more |
Product
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. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.
Reason for recall
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
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-2676-2017. 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.