FDAFebruary 22, 2023device

Automated Peritoneal Dialysis System. Used for automatic control of dialysis solution exchanges.

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

The hazard

The electrical safety testing was not properly performed on the impacted devices and additional testing is required

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

0085412676463

Recall history

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

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