GE Healthcare Recalls ADVANTX LCV+ Systems Due to CRT Monitor Fall Risk
GE Healthcare is recalling ADVANTX LCV+ systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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: The recall involves a risk-of-harm product (falling monitor) where injury has not yet been reported, fitting the 'High' severity criteria for theoretical or unreported injury risks.
Plain-English summary
GE Healthcare, LLC is conducting a recall of ADVANTX LCV+ systems due to the potential fall of aged CRT monitors. The recall also includes Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, and Innova 2000 systems.
A total of 1,598 units are affected, with 824 units in the United States and 774 units outside the US. The products were distributed across numerous US states and multiple international countries.
The recall is driven by the physical hazard of the monitors falling. No specific instructions for consumers are provided in the source text beyond the identification of the hazard.
The recalled product
- Product
- ADVANTX LCV+
- Manufacturer
- GE Healthcare, LLC
- Hazard
Distribution
Part of a larger recall action
This product is one of 13 recalled by GE Healthcare, LLC 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.
See all 13 products in this recall →Related recalls
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