FDAApril 16, 2024device

Product not distributed in the US. Implantable Cardioverter Defibrillators: a. VIVA QUAD XT CRT-D, Model Number DTBA2QQ. b. CLARIA MRI CRT-D SureScan, Model Number DTMA2D1. c. CLARIA MRI QUAD CRT-D SureScan, Model Number DTMA2QQ. d. AMPLIA MRI CRT-D SureScan, Model Number DTMB2D1. e. AMPLIA MRI C...

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

The hazard

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic

UPCs

007630006122690076300020628400763000206222007630002063070076300020629100763000206253007630002062460076300061183500763000206260007630002061470076300061219100763000206352

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →