YOGA MC24150ZRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886704079248), received between Mar 2, 2018 and Jul 26, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Physical Resistance” (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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 26, 2018Physical Resistance/Sticking; Physical Resistance/Sticking

  AS REPORTED BY A HEALTHCARE PROFESSIONAL, DURING A THROMBECTOMY OF THE MIDDLE CEREBRAL ARTERY (M1 SEGMENT), THE YOGA 24 150 CM (MC24150Z/UNK LOT) MICROCATHETER WAS DELIVERED TO THE DISTAL PORTION OF THE LESION AND THE 4.5 MM REVIVE SE (FRS21452299/UNK LOT) THROMBECTOMY DEVICE WAS INSERTED, BUT RESISTANCE WAS FELT AT THE INTERNAL CAROTID ARTERY AND THE REVIVE SE COULD NOT BE DELIVERED TO THE TARGET LESION. THE REVIVE SE THROMBECTOMY DEVICE BECAME STUCK IN THE YOGA 24 MICROCATHETER AND COULD NO LONGER BE ADVANCED. THEREFORE, THE SYSTEM WAS REMOVED FROM THE PATIENT AND THE DEVICES WERE REPLACED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT FURTHER INCIDENT. THE SURGERY WAS NOT DELAYED DUE TO THE EVENT. NO PATIENT COMPLICATIONS OCCURRED AS A RESULT OF THE EVENT. THE PATIENT¿S VESSEL WAS HEAVILY TORTUOUS. THE PRODUCTS WERE NEW AND STORED PER LABELING INSTRUCTIONS. THE PROCEDURE WAS CONDUCTED IN ACCORDANCE WITH THE INSTRUCTIONS FOR USE (IFU) AND A CONSTANT FLUSH WAS MAINTAINED. THE PRODUCTS WERE PREPPED ACCORDING TO THE IFU. NO VISIBLE PRODUCT DAMAGE WAS NOTED PRIOR TO AND FOLLOWING THE EVENT. THE USER DID NOT APPLY EXCESSIVE FORCE AT ANY TIME WHEN HANDLING THE PRODUCTS. THE PHYSICIA

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7723001 ↗
• MalfunctionMar 2, 2018Physical Resistance; Physical Resistance

  A REPORT WAS RECEIVED THAT DURING A THROMBECTOMY OF AN ACUTE ISCHEMIC STROKE AT THE M2 SEGMENT OF THE MIDDLE CEREBRAL ARTERY, THE REVIVE SE 4.5 MM OUS (FRS21452299/S12868) THROMBECTOMY DEVICE WAS INSERTED INTO THE YOGA 24 (MC24150Z/C42381) MICROCATHETER BUT GOT STUCK IN THE ¿INTRODUCER¿. THE DEVICE WAS REPLACED WITH A COMPETITOR DEVICE. THE PROCEDURE WAS DELAYED 10 MINUTES AS A RESULT OF THIS EVENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT FURTHER ISSUES. THERE WAS NO REPORT OF CONSEQUENCE OR IMPACT TO THE PATIENT. THE PATIENT¿S VESSEL WAS MILDLY TORTUOUS AND NOT CALCIFIED. AN ASAHI INTECC GUIDEWIRE AND AN OPTIMO (TOKAI MEDICAL PRODUCT) GUIDING CATHETER WERE ALSO USED FOR THE CASE. THE COMPLAINT PRODUCTS WERE NEW AND STORED PER LABELING INSTRUCTIONS. THE PROCEDURE WAS CONDUCTED IN ACCORDANCE WITH THE INSTRUCTIONS FOR USE (IFU) AND A CONSTANT FLUSH WAS MAINTAINED. NO VISIBLE PRODUCT DAMAGE WAS NOTED PRIOR TO THE EVENT. THE PRODUCTS WILL BE RETURNED FOR ANALYSIS. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7309049 ↗