YOGA MC24150ZBRecalls & reported problems
Medos International Sàrl · YOGA 24XB Microcatheter 0.024 Inch I.D. - 150cm - Straight 2.7F (0.92mm) 2.4F (0.82mm) 0.024 Inch (0.61mm) Contents: 1 Microcatheter and 1 Shaping Mandrel · Class 2
Data updated Oct 13, 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 10886704079255), received between Mar 1, 2018 and Mar 1, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Obstruction of Flow” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Obstruction of Flow1
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 1, 2018Obstruction of Flow; Obstruction of Flow
AS REPORTED BY AN AFFILIATE, DURING A COIL EMBOLIZATION OF AN ANEURYSM FOR THROMBUS RECOVERY AT THE MIDDLE CEREBRAL ARTERY (M1), A REVIVE SE THROMBECTOMY DEVICE (FRS21452299, S12435) WAS INSERTED INTO THE YOGA MICROCATHETER (MC24150Z, C42381) BUT THERE WAS STRONG RESISTANCE FELT IN THE CATHETER. THEREFORE, THE STENT WAS REPLACED WITH ANOTHER ONE (SOLITAIRE). HOWEVER, IT COULD NOT BE REACHED TO THE LESION ALTHOUGH IT WAS MORE ADVANCED THAN THE REVIVE. THEREFORE, THE MICRO CATHETER WAS REPLACED WITH A NON-CERENOVUS MICROCATHETER. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT FURTHER ISSUES OR DELAY. THERE WAS NO PATIENT INJURY OR COMPLICATIONS REPORTED. THE PRODUCTS ARE NOT AVAILABLE FOR THE INVESTIGATION. THE PRODUCTS WERE NEW AND STORED PER LABELING INSTRUCTIONS. THE PROCEDURE WAS CONDUCTED IN ACCORDANCE WITH THE INSTRUCTIONS FOR USE (IFU) AND CONSTANT FLUSH HAD BEEN MAINTAINED AT ALL TIME. NO VISIBLE DEFECT/DAMAGE WAS NOTED ON THE PRODUCTS PRIOR TO THE EVENT. IT WAS A CASE THAT THERE WAS HEAVILY TORTUOUSNESS DUE TO BOVINE AND DIFFICULT TO APPROACH. NO REPORT OF THE OTHER DEVICE USED IN THE PROCEDURE IS AVAILABLE. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7307569 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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