Z-2430-2023 Class II Ongoing

Recalled by ICU Medical Inc — Lake Forest, IL

Recall Details

Product Type
Devices
Report Date
August 30, 2023
Initiation Date
July 13, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
93135 devices

Product Description

Plum 360 Infusion System, List Numbers: 300100405, 300100409, 300100413, 300100414, 300100415, 300100418, 300100451, 300100452, 300100453, 300100481, 300100483, 300100613, 300101013, 300101113, 300101114, 300101313, 300101379, 300102213, 300102713, 300102913, 300103413, 300103414, 300104213, 300105413, 300105713, 300106313, 300106513, 300106581, 300107813, 300107814, 300108513, 300108813, 300108814, 300109913; infusion pump

Reason for Recall

Due to a manufacturing defect of a supplier provided component, there is a potential that the audible signal for an alarm may not sound under certain conditions.

Distribution Pattern

Worldwide

Code Information

UDI/DI M335300101, All Plum 360 pumps manufactured between July 2020 and December 2021