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
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 · TerminatedMedtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375
- Z-1245-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35
- Z-1248-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30
- Z-1246-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40
- Z-0205-2015 · Oct 13, 2014 · TerminatedMedtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
- Z-1564-2013 · Jun 12, 2013 · TerminatedMedtronic, 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 · TerminatedCATHETER 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 · TerminatedCATHETER 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 · TerminatedCATH. 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 · TerminatedCATHETER 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 · TerminatedCATH. 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 · TerminatedCATH. 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 · TerminatedCATH. 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 · TerminatedCATHETER 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 · TerminatedCATHETER 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.
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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