CEREGLIDE NIC57137URecalls & reported problems
Cerenovus, Inc. · CEREGLIDE 57 · Class 2
All models of CEREGLIDE (6)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886704086550), received between Dec 18, 2025 and Dec 18, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (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.
Reports received per month
Most reported problems
Device problems
- Deformation Due to Compressive Stress1
- Physical Resistance/Sticking1
Patient problems
- Thromboembolism1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 18, 2025Deformation Due to Compressive Stress; Physical Resistance/Sticking; Deformation Due to Compressive Stress; Physical Resistance/Sticking
THE HEALTHCARE PROFESSIONAL REPORTED THAT DURING A THROMBECTOMY PROCEDURE TO TREAT AN ACUTE ISCHEMIC STROKE (AIS) TARGETING AN OCCLUSION IN THE A2 SEGMENT OF THE RIGHT ANTERIOR CEREBRAL ARTERY (ACA), A CEREBASE, A 137 CM CEREGLIDE 57 CATHETER (NIC57137U / 31766662), AN ARISTOTLE® 18 GUIDEWIRE (SCIENTIA VASCULAR) WERE USED TO NAVIGATE TO THE CLOT FACE. AFTER ONE (1) PASS, A MAJORITY OF THE CLOT WAS REMOVED BUT SOME CLOT HAD MIGRATED DISTAL INTO THE A3 SEGMENT. THE CEREGLIDE 57 CATHETER WAS THEN TRACKED UP AGAIN, BUT IT WAS UNABLE TO REACH THE DISTAL CLOT AND A 160CM CEREGLIDE 42 CATHETER (NIC42160U / 31766628) WAS USED TO REACH THE CLOT. IT WAS REPORTED THAT DURING THE ATTEMPT TO INSIDER THE CEREGLIDE 42 INTO THE CEREGLIDE 57, THE CEREGLIDE 42 WAS UNABLE TO TRAVERSE PAST THE HUB OF THE CEREGLIDE 57. IT WAS NOTED THAT THERE WAS A SMALL KINK IN THE CEREGLIDE 57 CATHETER, BUT IT WAS MUCH MORE DISTAL TO THE HUB OF THE DEVICE, AND IT WAS NOT THE CAUSE OF THE CEREGLIDE 42 CATHETER NOT FITTING INTO THE CEREGLIDE 57 CATHETER. AFTER MANY UNSUCCESSFUL ATTEMPTS OF TRYING TO PUT THE CEREGLIDE 42 INTO THE CEREGLIDE 57, THE PHYSICIAN PULLED THE CEREGLIDE 57 OUT AND TRAVERSED UP TO THE CLOT USING
Patient problems: Thromboembolism
MAUDE report 23843470 ↗
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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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