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

Recall Z-1011-2025 — Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

U.S. FDA — Device Enforcement · United States · 2024-12-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1011-2025
Date of alert
2024-12-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00085412486512
Reported risk: Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
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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