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

Recall Z-1418-2025 — Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086

U.S. FDA — Device Enforcement · United States · 2025-02-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1418-2025
Date of alert
2025-02-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00887761974074
Reported risk: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
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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