FDA recall Z-1254-2025

Baxter Healthcare Corporation · Class I · device

Product

Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

Reason for recall

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

Distribution

US: Nationwide

Key facts

Status: Ongoing
Initiation date: 2025-02-05
Report date: 2025-03-12
Voluntary/Mandated: Voluntary: Firm initiated
Location: Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1254-2025