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FDAFebruary 6, 2017device

Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems — Recall Details · AllClear