FDADecember 22, 2023device

Baxter Exactamix Pro 1200, REF EXM12DY

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

05413765588150

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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