FDAJuly 31, 2024device

Inspire Model 4063 Stimulation Lead, component of the Inspire Upper Airway Stimulation (UAS) system.

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

The hazard

Labeling error with a mismatch between the shelf box serial number label and the serial number of the lead provided in the box.

What to do

FDA enforcement status: Ongoing

Brands named

inspire medical systemsinspireinspire medical

UPCs

10855728005793

Recall history

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

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Inspire Model 4063 Stimulation Lead, component of the Inspire Upper Airway Stimulation (UAS) system. — Recall Details · AllClear