FDAFebruary 1, 2013device
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 chann...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
What to do
FDA enforcement status: Terminated
Brands named
icu
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAPlum Solo Precision IV Pump, 40001-04012026-04-29
- FDAPlum Duo Infusion Pump, 40002-04012026-04-29
- FDAPlum Duo Precision IV Pump, 40002-04032026-04-29
- FDAOncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL39602026-03-24
- FDATego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D10002025-12-19
- FDAPortex Spinal Tray, Item No. A3729-24 A35952025-12-19
- FDAPulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG2025-12-19
- FDAPlum Duo Infusion System, List Number 40002-04-012025-12-15
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