FDAJune 12, 2018device

Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep Apnea, Inspire Part #900-003-020, Product Usage: The device is an implanted component of the Inspire Upper Airway Stimulation (UAS) system. The UAS therapy is used to treat a subset of patients with moderate to severe o...

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

The hazard

Incorrect use-by date on the device registration/patient file labels.

What to do

FDA enforcement status: Terminated

Brands named

inspire medical systemsinspireinspire medical

UPCs

10855728005434

Recall history

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

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