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

Recall Z-2530-2024 — Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2

U.S. FDA — Device Enforcement · United States · 2024-06-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2530-2024
Date of alert
2024-06-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Reported risk: Improperly performed testing prior to release
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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