Launcher LA6SAL10SHRecalls & reported problems
Medtronic, Inc. · CATHETER LA6SAL10SH LA 6F 100CM SAL10 · 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 00613994819499), received between Mar 6, 2020 and Mar 6, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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.
Most reported problems
Device problems
- Material Deformation1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2020Material Deformation; Material Deformation
A LAUNCHER GUIDE CATHETER WAS USED DURING A PROCEDURE TO TREAT A NON-CALCIFIED, NON-TORTUOUS LESION IN THE MID RIGHT CORONARY ARTERY (RCA). THERE WAS NO DAMAGE NOTED TO THE PACKAGING. THE DEVICE WAS REMOVED FROM PACKAGING PER IFU WITH NO ISSUES. THE DEVICE WAS INSPECTED WITH NO ISSUES. THE DEVICE WAS PREPPED PER IFU WITH NO ISSUES. RESISTANCE WAS NOT ENCOUNTERED. EXCESSIVE FORCE WAS NOT USED. IT WAS REPORTED THAT THERE WAS SHARP CORNER NOTED ON THE TIP OF THE DEVICE. AFTER THE SHARP CORNER WAS NOTED, THE PHYSICIAN SHAPED THE TIP INTO A CYLINDRICAL SHAPE. THE PATIENT IS ALIVE WITH NO INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9797341 ↗
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-1248-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30
- Z-1245-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35
- 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-0953-06 · Apr 5, 2006 · TerminatedCATH.GUIDE 6F JR 4.0 SH 110CM CATHETER LA6JR40SHA LA 6F 110CM JR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are
- Z-0963-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F SR4.5 LAUNCHER CATHETER LA6SR45 LA 6F 100CM SR45 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are int
- 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-0951-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F JL5.0 110CM LAU CATHETER LA6JL50A LA 6F 110CM JL50 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are i
- Z-0968-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F SR6.0 W/SH LAUN Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peri
- Z-0956-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F SR3.0 LAUNCHER CATHETER LA6SR30 LA 6F 100CM SR30 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are int
- Z-0942-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F EBU3.5 110CM LA CATHETER LA6EBU35A LA 6F 110CM EB35 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-0967-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F SR6.0 LAUNCHER CATHETER LA6SR60 LA 6F 100CM SR60 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are int
…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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