Device product
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
Z-2430-2023
Product summary
- Firm
- ICU Medical Inc
- Event
- Event 92630
- Status
- Ongoing
- Classification
- Class II
- Quantity
- 93135 devices
- Official record key
device-enforcement:Z-2430-2023
Official wording
Reason: 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.
Code information: UDI/DI M335300101, All Plum 360 pumps manufactured between July 2020 and December 2021
Distribution pattern: Worldwide
Derived failure modes
-
Manufacturing or process control
manufacturing defect