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

Recall Z-0080-2015 — 15 L Cycler Drainage Bag Product Usage: For use with Baxter Cycler Tubing sets as a peritoneal dialysis accessory.

U.S. FDA — Device Enforcement · United States · 2013-10-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0080-2015
Date of alert
2013-10-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corp
Product category
device
Product type
Devices
Reported risk: The large tube clamp used to close the drain tube on the 15 L Cycler Drainage Bag may not fully close the drain tube and may result in leakage.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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