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Launcher LA6JL50Recalls & reported problems

Medtronic, Inc. · CATHETER LA6JL50 LA 6F 100CM JL50 · Class 2

All models of Launcher (64)

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 00763000392536), received between May 9, 2025 and May 9, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (1 report).

52 other recalls cover devices cleared under the same FDA submission (K021256); they may or may not involve this specific model.

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 1 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Use of Device 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.

  • MalfunctionMay 9, 2025Use of Device Problem; Use of Device Problem

    IT WAS REPORTED THAT THE SHELF LIFE OF ONE 6F LAUNCHER GUIDE CATHETER WAS EXPIRED NINETEEN DAYS WHEN IT WAS USED. THE DEVICE WAS INSPECTED PRIOR TO USE AND PREPPED PER IFU WITH NO ISSUES NOTED. THE LESION BEING TREATED WAS NON-TORTUOUS, NON-CALCIFIED LOCATED IN THE DISTAL FEMORAL ARTERY. THERE WAS NO PATIENT INJURY OR MEDICAL-SURGICAL INTERVENTIONS AS A RESULT OF THE EVENT. THE PATIENT'S CURRENT HEALTH STATUS IS DESCRIBED AS WELL. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21992062 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K021256. One submission often covers many models, so check the product and lot details in each record.

  • Z-1247-2021 · Jan 15, 2021 · Terminated
    Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375
  • Z-1245-2021 · Jan 15, 2021 · Terminated
    Medtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35
  • Z-1248-2021 · Jan 15, 2021 · Terminated
    Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30
  • Z-1246-2021 · Jan 15, 2021 · Terminated
    Medtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40
  • Z-0205-2015 · Oct 13, 2014 · Terminated
    Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
  • Z-1564-2013 · Jun 12, 2013 · Terminated
    Medtronic, Launcher Guiding Catheter, Model # LA8EBU45SH, Lot # 0006722866, 8F and Model # LA6IMAD, Lot # 0006724224, 6F Product Usage: The Medtronic Guiding Catheter is designe
  • Z-1000-06 · Apr 5, 2006 · Terminated
    CATHETER SA6SR50 SA 6F 100CM Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peri
  • Z-0950-06 · Apr 5, 2006 · Terminated
    CATHETER LA6JL45A 6F 110CM JL4 CATHETER LA6JL45A 6F 110CM JL45 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are intr
  • Z-0943-06 · Apr 5, 2006 · Terminated
    CATH. GUIDE 6F EBU4.0 110CM LA CATHETER LA6EBU40A LA 6F 110CM EB40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are
  • Z-1001-06 · Apr 5, 2006 · Terminated
    CATHETER SB63DRC SB 6F 100CM 3 CATHETER SB63DRC SB 6F 100CM 3DRC Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are in
  • Z-0958-06 · Apr 5, 2006 · Terminated
    CATH. GUIDE 6F SR3.5 LAUNCHER CATHETER LA6SR35 LA 6F 100CM SR35 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are int
  • Z-0938-06 · Apr 5, 2006 · Terminated
    CATH. GUIDE 6F 3DRC W/SH LAUNC CATHETER LA63DRCSH LA 6F 100CM 3DRC Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are
  • Z-0948-06 · Apr 5, 2006 · Terminated
    CATH. GUIDE 6F JL4.0 110CM LAU CATHETER LA6JL40A LA 6F 110CM JL40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are i
  • Z-1002-06 · Apr 5, 2006 · Terminated
    CATHETER SB63DRCSH SB 6F 100CM Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peri
  • Z-1006-06 · Apr 5, 2006 · Terminated
    CATHETER SB6SR40 SB 6F 100CM S CATHETER SB6SR40 SB 6F 100CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are in

…and 37 more.

Other Catheter, percutaneous devices

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Sources and updates

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