---
title: "COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardiove... — FDA record Z-2190-2024 | Is It on Recall"
description: "Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing."
url: https://isitonrecall.com/recall/fda-device-z-2190-2024-cobalt-hf-quad-crt-d-mri-surescan-model-number-dtpb2qq-implantable-cardioverter-defibrillator/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator — FDA record Z-2190-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 16, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator
- **Reason**: Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
- **Classification**: Class II
- **Recalling firm**: Medtronic Inc.
- **Quantity**: 14
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2190-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2190-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | GTIN: 00763000178192, Serial Numbers: RTK624593S, RTK624594S, RTK624595S, RTK624596S, RTK624597S, RTK624599S, RTK624601S, RTK624602S, RTK624603S, RTK624604S, RTK624606S, RTK624607S; GTIN: 00763000711207, Serial Numbers: RTK624400S, RTK624405S. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the states of CA, CT, FL, IN, MA, MI, NC, NH, NJ, NM, NY, OH, TX, VA and the countries of Australia, Austria, Bulgaria, Canada, China, Croatia, Czech Republic, France, Georgia, Germany, Greece, Guadeloupe, Iceland, Ireland, Italy, Jordan, Kosovo, Latvia, Moldova, Republic Of, Netherlands, Northern Ireland, Norway, Oman, Panama, Poland, Portugal, Qatar, Reunion, Slovakia, Slovenia, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jul 3, 2024
- **Recall initiation date**: Apr 16, 2024
- **Center classification date**: Jun 26, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2190-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Inc records](https://isitonrecall.com/brand/medtronic-inc/)
