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Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)
Recalled October 28, 2020 · FDA recall Z-0122-2021 · Baxter Healthcare
Hazard
Baxter is updating the device IFU for safety communication regarding cleaning practices. · FDA Class I
Units
152,539 units
Sold at
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)
Description
Baxter is updating the device IFU for safety communication regarding cleaning practices.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →