FDADecember 18, 2015device

VNS Therapy AspireSR Generator Model 106. Indicated for use as an adjunctive therapy in reducing the frequency of seizures.

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

The hazard

Recall being initiated in response to three reports of "Burst Watchdog Timeout" events occurring with the Model 106 AspireSR Generator, resulting in a device reset condition where stimulation output is disabled.

What to do

FDA enforcement status: Terminated

Brands named

cyberonics

UPCs

05425025750061

Recall history

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

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