RAPIDTRANSIT 601-240Recalls & reported problems
Medos International Sàrl · RAPIDTRANSIT Infusion Catheter TIP MARKERS 1 USABLE LENGTH 100 cm DISTAL LENGTH 30 cm DISTAL OD 2.3F (0.75 mm) 2.8F (0.95 mm) .021 Inch (0.5 mm) Contents: 1 Infusion Catheter and 1 Shape Mandrel. Minimum Guiding Catheter I.D. / Dia. .042 Inch (1.1 mm) · Class 2
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 10886704028338), received between Nov 4, 2019 and Nov 4, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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
- Physical Resistance/Sticking1
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.
MalfunctionNov 4, 2019Physical Resistance/Sticking; Physical Resistance/Sticking
AS REPORTED BY A HEALTHCARE PROFESSIONAL, THERE WAS RESISTANCE BETWEEN A 100CM RAPIDTRANSIT MICROCATHETER (601240, 17659684) AND AN UNKNOWN GUIDEWIRE. THE MICROCATHETER (MC) WAS REMOVED FROM THE PATIENT¿S BODY AND FLUSHED. IT WAS INSERTED AGAIN BUT THE SAME ISSUE CONTINUED. IT WAS REPLACED WITH ANOTHER DEVICE AND THE PROCEDURE WAS CONTINUED. THE CUSTOMER STATES THERE IS NO ADDITIONAL INFORMATION AVAILABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9272102 ↗
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- MarksmanTM FA-55150-1030Micro Therapeutics, Inc. · Catheter, continuous flush109 reports
- Renegade™ HI-FLO™ Kit M001183020Boston Scientific Corporation · Catheter, continuous flush109 reports
- EkoSonic® 6779-002Boston Scientific Corporation · Catheter, Continuous Flush1 recall4 deaths56 reports
- Chameleon CH08-40-75USMozarc Medical US LLC · Catheter, continuous flush2 recalls4 reports
- RebarTM 105-5081-153Micro Therapeutics, Inc. · Catheter, continuous flush2 deaths102 reports
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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