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

Recall Z-0215-2025 — Baxter Operating Table TruSystem 7000 (MBW) V, Product code REF 1841082

U.S. FDA — Device Enforcement · United States · 2024-09-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0215-2025
Date of alert
2024-09-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00887761974234
Reported risk: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
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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