Conservia™ M0068502210Recalls & reported problems
Boston Scientific Corporation · Transvaginal Mid-Urethral Sling · 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 08714729855996), received between Oct 24, 2024 and Oct 24, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Movement Disorder1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 24, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT SEVERAL MONTHS AGO, THE PATIENT HAD PAIN IN THE RIGHT SIDE OF THE VAGINAL, EXTREME GROIN PAIN, AND PINCHING SENSATION THAT PREVENTED HER FROM WALKING. THE PATIENT STILL EXPERIENCED EXTREME GROIN PAIN AND WALKING PROBLEMS. IT WAS NOTED THAT THE PATIENT WAS LOOKING INTO REMOVING THE DEVICE.
Patient problems: Movement Disorder; Pain
MAUDE report 20528579 ↗
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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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