FDAJune 29, 2015device
Baxter HomeChoice and HomeChoice Pro APD systems, designed to provide Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Loud operating sounds, which was unacceptable to the end users when the device was powered on. The HomeChoice devices continue to perform as intended, as the issue is only associated with the noise coming from the device and not the function of it. May delay treatment if changing to a different system.
What to do
FDA enforcement status: Terminated
Brands named
baxter healthcarebaxter
Recall history
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