FDAJuly 7, 2022device

The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. The software in use controls all communication functions for the pulse generator.

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

The hazard

There is potential for unanticipated software anomalies to occur when using the Model 2868 Application loaded on the 3120 ZOOM LATITUTDE programmer when communicating with certain Boston Scientific transvenous defibrillators.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

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Recall history

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

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The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. The software in use controls all communication functions for the pulse generator. — Recall Details · AllClear