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
- Affected units
- 1,077
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.
Part of a larger recall action
This product is one of 9 recalled by Baxter Healthcare Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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