Medtronic recalls specific Implantable Cardioverter Defibrillators (COBALT HF QUAD CRT-D MRI SureScan) with model DTPB2QQ due to potential welding cracks causing failure during manufacturing leak checks.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Medtronic is recalling certain Implantable Cardioverter Defibrillators (ICDs) that may have a welding crack causing failure during manufacturing. This defect could lead to device malfunction, but the recall does not specify a risk of serious injury or death in normal use.
The devices may have a welding crack that causes failure during the leak check step in manufacturing. This defect could lead to device malfunction, but the recall does not indicate a risk of serious injury or death in normal use.
People with the specific model DTPB2QQ Implantable Cardioverter Defibrillators (ICDs) listed in the recall. Those with the serial numbers provided are most at risk.
Check if your device has the model number DTPB2QQ and the specific serial numbers listed in the recall. The devices were sold with GTIN 00763000178192 or 00763000711207.
Review your device's model number and serial numbers to confirm if it matches the recalled items listed in the notice.
The recall states a potential manufacturing defect that could cause device failure during leak checks, but it does not specify a risk of serious injury or death in normal use.
Check if your device has the model number DTPB2QQ and the specific serial numbers listed in the recall notice (RTK624593S through RTK624607S).
The recall does not provide a remedy or action steps for affected devices. You should contact Medtronic directly for further instructions.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2190-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2190-2024 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
