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Baxter Healthcare Corporation recalls Prismaflex Control Unit
Recalled May 27, 2020 · FDA recall Z-2066-2020 · Baxter Healthcare
Hazard
Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed. · FDA Class II
Units
5 devices US territories
Sold at
Distribution only to Puerto Rico and Guam
Description
Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.
Product
Prismaflex Control Unit
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →