Launcher LA6JL30Recalls & reported problems
Medtronic, Inc. · CATHETER LA6JL30 LA 6F 100CM JL30 · 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 00613994818126), received between May 10, 2017 and May 10, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Expiration Issue” (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
- Device Expiration Issue1
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.
MalfunctionMay 10, 2017Device Expiration Issue; Device Expiration Issue
THE LAUNCHER GUIDE CATHETER WAS REMOVED FROM PACKAGING PER IFU WITH NO ISSUES NOTED. AFTER CATHETER HAD BEEN USED, IT WAS NOTICED THAT IT WAS EXPIRED FOR 8 DAYS. THE EVENT DID NOT LEAD TO OR EXTEND PATIENT HOSPITALIZATION. NO INJURY REPORTED. THE HOSPITAL DIDN'T KEEP THE CATHETER.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6556745 ↗
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-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-1248-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30
- Z-1247-2021 · Jan 15, 2021 · TerminatedMedtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375
- 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-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
- 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-0960-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F SR4.0 LAUNCHER CATHETER LA6SR40 LA 6F 100CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are int
- Z-0946-06 · Apr 5, 2006 · TerminatedCATH. GUIDE 6F JL3.5 110CM LAU CATHETER LA6JL35A LA 6F 110CM JL35 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are i
- Z-1004-06 · Apr 5, 2006 · TerminatedCATHETER SB6SR35 SB 6F 100CM S Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peri
- Z-1005-06 · Apr 5, 2006 · TerminatedCATHETER SB6SR35SH 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-0955-06 · Apr 5, 2006 · TerminatedCATHETER LA6MB1A LA 6F 110CM M Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peri
- Z-0961-06 · Apr 5, 2006 · TerminatedCATHETER LA6SR40A 6F 110CM SR4 CATHETER LA6SR40A 6F 110CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are intr
- 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
…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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