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ICU recalls The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies a
Recalled July 19, 2017 · FDA recall Z-2683-2017 · ICU
Hazard
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues. · FDA Class II
Units
363892 units
Sold at
Nationwide, Worldwide
Description
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
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.
Manufacturer(s)
ICU
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →