Ventix® Link Knotless Anchor 110025992Recalls & reported problems
Cayenne Medical, Inc. · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887868269387), received between May 5, 2020 and May 5, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Migration” (2 reports).
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 18, 2026.
Most reported problems
Device problems
- Migration2
Patient problems
- No Code Available2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 5, 2020Migration; Migration
IT WAS REPORTED THAT PATIENT UNDERWENT REVISION SURGERY DUE TO ANCHOR MIGRATION. IT WAS ALSO REPORTED BY THE HCP THAT THERE WAS NOTHING WRONG WITH THE DEVICE. NO OTHER PATIENT HARM WAS REPORTED.
Patient problems: No Code Available
MAUDE report 10027058 ↗InjuryMay 5, 2020Migration; Migration
IT WAS REPORTED THAT PATIENT UNDERWENT REVISION SURGERY DUE TO ANCHOR MIGRATION. IT WAS ALSO REPORTED BY THE HCP THAT THERE WAS NOTHING WRONG WITH THE DEVICE. NO OTHER PATIENT HARM WAS REPORTED.
Patient problems: No Code Available
MAUDE report 10026552 ↗
Other Fastener, Fixation, Nondegradable, Soft Tissue devices
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- OMNISPAN ORTHOCORD 228142Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE932 reports
- FOOTPRINT 72202901Smith & Nephew, Inc. · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE721 reports
- RIGIDLOOP 232447Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE633 reports
- Arthrex® AR-3636Arthrex, Inc. · Fastener, fixation, nondegradable, soft tissue624 reports
- OMNISPAN ORTHOCORD 228141Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE609 reports
- TRUESPAN ORTHOCORD 228162Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE460 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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