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Baxter Healthcare ExactaMix Pro 1200 and Pro 2400 Recalled Due to a Software Error
Baxter Healthcare is recalling the ExactaMix Pro 1200 and the Pro 2400 because of a software error that can cause more ingredients than needed to be added to the final solution. An issue was identified in software versions 2.0.8 and 2.1.8 while using the “Use Some Overfill” feature, potentially resulting in extra ingredients being delivered. Baxter is working on a software update to fix this issue, and it's expected to be available in March 2024.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Please be aware, this recall is a correction, not a product removal.
Questions?
If you have questions about this recall, contact Baxter Global Technical Services at 1-800-678-2292.
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