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Attain Command™ + SureValve™ 6250V-MB2Recalls & reported problems

Medtronic, Inc. · CATHETER 6250V-MB2 ATTAIN COMMAND · Class 2

All models of Attain Command + SureValve (17)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000160302), received between Jun 8, 2021 and Jun 8, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Integrity Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Material Integrity Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 8, 2021Material Integrity Problem; Material Integrity Problem

    IT WAS REPORTED THAT THE PHYSICIAN EXPERIENCED DIFFICULTY WHEN BEGINNING TO SLIT THE HUB OF THE DELIVERY CATHETER AND THE SLITTER KEPT GETTING STUCK. THREE DIFFERENT SLITTERS WERE USED AND THE PHYSICIAN WAS ULTIMATELY ABLE TO SLIT THE CATHETER. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11956400 ↗

Other Catheter, percutaneous devices

All Catheter, percutaneous devices →

Sources and updates

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