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Baxter Healthcare Corporation recalls Baxter Exactamix Pro 2400, REF EXM24DY
Recalled February 28, 2024 · FDA recall Z-1002-2024 · Baxter Healthcare
Hazard
An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume. · FDA Class I
Units
67 devices
Sold at
US: AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OR, SD, TX, WA, WI,
Description
An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.
Product
Baxter Exactamix Pro 2400, REF EXM24DY
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →