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Recall Observatory FDA recall evidence

Device product

COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator

Z-2190-2024

April 16, 2024

Class II

Product summary

Firm
Medtronic Inc.
Event
Event 94674
Status
Ongoing
Classification
Class II
Quantity
14
Official record key
device-enforcement:Z-2190-2024

Official wording

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

Code information: GTIN: 00763000178192, Serial Numbers: RTK624593S, RTK624594S, RTK624595S, RTK624596S, RTK624597S, RTK624599S, RTK624601S, RTK624602S, RTK624603S, RTK624604S, RTK624606S, RTK624607S; GTIN: 00763000711207, Serial Numbers: RTK624400S, RTK624405S.

Distribution pattern: 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.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing defect