Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1292-2015 — The HomeChoice Pro APD System is a peritoneal dialysis system. The HomeChoice Pro Automated Personal Cycler peritoneal dialysis system is intended for automatic control of dialysate solution exchange in the treatment of pediatric and adult renal failure patients undergoing peritoneal dialysis.

U.S. FDA — Device Enforcement · United States · 2013-10-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1292-2015
Date of alert
2013-10-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corp.
Product category
device
Product type
Devices
Reported risk: The occluder in affected devices 1) may have sharp edges that could cut the pneumatic tubing that connects the occluder blade to the manifold causing an unrecoverable system error, and/or 2) blade may separate from the back plate and cause Slow / No Flow alarm requiring therapy termination.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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