Product Safety Recalls

Product Recall Tracker

Baxter Healthcare Corporation Recall 88073

Description: Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids.

Baxter Healthcare Corporation Recall 88073 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-2110-2021
Event ID88073
Event DescriptionSpectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids.
Product TypeDevices
DistributionUnited States (including Puerto Rico), Canada, Bahamas, Bermuda, Guyana, and Trinidad and Tobago.
Quantity130135 units
Recall ReasonSystem errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System performance anomalies resulted in excessive Spectrum IQ pump connectivity errors.
Device Classification20210818
Device Code InfoAll Serial Numbers
Center Classification Date20210806
Recall Initiation Date20210604
Recalling FirmBaxter Healthcare Corporation
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.