CASHMERE SRC140717-20Recalls & reported problems
Medos International Sàrl · CASHMERE microcoil CASHMERE 14 Stretch Resistant Coil 7mm x 17cm 190cm Contents: 1 Detachable Coil System · Class 2 · Implant
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 00878528004028), received between Aug 27, 2019 and Aug 27, 2019 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Headache1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 27, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WHO UNDERWENT A COIL EMBOLIZATION PROCEDURE THAT TARGETED A BASILAR ANEURYSM TWO YEARS AGO IN 2017, REACHED OUT TO A SALES REP TO REPORT THAT SHE IS SUFFERING FROM A HEADACHE THAT HAS TURNED INTO A CHRONIC, PERMANENT HEADACHE. THE PATIENT WOULD LIKE TO KNOW THE MATERIAL COMPOSITION OF THE 7 MM X 17 CM CASHMERE 14 STRETCH RESISTANT COIL (SRC14071720 / LOT #: UNK) WITH RESPECT TO A POTENTIAL INTOLERANCE / ALLERGY.
Patient problems: Headache
MAUDE report 8936569 ↗
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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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