ClearanceBrief
Recall Z-1565-2023 ยท FRN Pump, Infusion

ICU Medical Inc

Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010

DateMay 16, 2023 (initiated Mar 22, 2023)
StatusOpen, Classified
ReasonDue to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease earlier in the battery lifecycle than expected.
Root causeUnder Investigation by firm
ActionICU medical issued an URGENT: MEDICAL DEVICE CORRECTION notice on 03/22/2023 to its direct and indirect consignees by mail. The notice explained the issue and the hazard and requested the following: Clinical Users: Whenever possible, keep the pump plugged into AC power. Before disconnecting the pump from AC power, please ensure that the battery is fully charged. Closely monitor the Battery Status Indicator while the pump is disconnected from AC power. Additionally, have a backup pump available when infusing critical medications. Biomedical Engineering: You may replace affected batteries
Quantity28656 units
Distributionworldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K141789PLUM 360 INFUSION SYSTEM WITH HOSPIRA MEDNET, SMART CARD PLUG N PLAY CE 3.0 MODULE FOR PLUM A+ INFUSION SYSTEM UPGRADE
Hospira, Inc., Jan 16, 2015
K161469Plum 360(TM) Infusion System with MedNet/ Smart Card Plug and Play Module
Hospira, Inc., Mar 28, 2017