Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Baxter Exactamix Pro 1200 Recalled by Baxter Healthcare Corporation Due to An error was identified in software versions 2.0.8...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.
Affected Products
Baxter Exactamix Pro 1200, REF EXM12DY
Quantity: 8 devices
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 22 states: AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NE, NV, NH, NJ, NY, NC, OR, SD, TX, WA, WI
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report