The Recall Desk
HighFDA (Devices)·Z-0213-2025·Announced 2024-10-30

Baxter Operating Table TruSystem 7000 recalled for electrical hazard

Baxter is recalling 1,077 TruSystem 7000 operating tables worldwide due to electrical short-circuits and smoke emissions in battery connectors reported by customers.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is a risk-of-harm medical device with documented electrical failures (short-circuits, smoke emissions) creating potential fire and electrocution hazards. Per the severity rubric, risk-of-harm products without confirmed patient injury score at level 3 (High).

Plain-English summary

Baxter Healthcare Corporation is recalling the TruSystem 7000 operating table (Product Code REF 1841049, UDI/DI 00887761968691, all serial numbers). The recall affects 1,077 units distributed worldwide.

Customers have reported electrical short-circuits and smoke emissions in the device batteries and their connectors. These electrical failures pose a risk of fire and electrocution in the operating room environment.

The recalled product

Product
Baxter Operating Table TruSystem 7000 (dV), Product code REF 1841049
Manufacturer
Baxter Healthcare Corporation
Hazard
  • electrical-short-circuit
  • smoke-emission
  • fire-risk
  • electrocution-risk

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • UDI/DI00887761968691
  • All Serial Numbers

Distribution

Distribution scope not specified by the agency.