FDAJune 18, 2019device

Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes

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

The hazard

Supplemental information provided with devices indicates that the subdural electrodes, depth electrodes, and anchor bolts are approved for use in the MR environment, for which they are not approved for such use.

What to do

FDA enforcement status: Terminated

Brands named

ad tech medical instrument

Recall history

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

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