Home / Recalls / Baxter Healthcare Corporation / Z-0123-2021

Z-0123-2021 Class I Terminated

Recalled by Baxter Healthcare Corporation — Deerfield, IL

Recall Details

Product Type
Devices
Report Date
October 28, 2020
Initiation Date
June 30, 2020
Termination Date
April 29, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
146,224 units

Product Description

Spectrum IQ Infusion System with Dose IQ Safety Software

Reason for Recall

Baxter is updating the device IFU for safety communication regarding cleaning practices.

Distribution Pattern

Distribution throughout the United States, St. Thomas USVI, and Puerto Rico. Foreign distribution including Canada, Caribbean (Barbados, Trinidad and Tobago, Jamaica, Bahamas, Bermuda, and Guyana)

Code Information

Product Code: 3570009, All Serial Numbers; GTIN 00085412610900

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