FDAAugust 20, 2024device

Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device

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

The hazard

Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounders. Particulate matter has been observed within the inlet primary packaging inlet components, including within the sterile fluid path tubing, before use.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

00085412475806

Recall history

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

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