FDAApril 7, 2021device

Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D) - Product Usage: are multiprogrammable cardiac devices that monitor and regulate a patient s heart rate by providing single- or dual chamber rate responsive bradycardia pacing, cardi...

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

The hazard

The device may contain a manufacturing defect of a missing resistance spot weld (RSW).

What to do

FDA enforcement status: Terminated

Brands named

medtronic inc cardiac rhythm and heart failure crhfmedtronicmedtronic inc

UPCs

00763000178215

Recall history

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

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