Tenolok T50S (UDI 10845854043783)Recalls & reported problems
Conmed Corporation · 5.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854043783), received between May 22, 2019 and May 22, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Human-Device Interface Problem” (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
Device problems
- Human-Device Interface Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2019Human-Device Interface Problem; Human-Device Interface Problem
THE CONMED REPRESENTATIVE REPORTED ON BEHALF OF THE FACILITY THAT THE SURGEON HAD IMPLANTED AN EXPIRED T50S, 5.0MM TENOLOCK ANCHOR DURING A BICEPS TENDONESIS SURGERY ON (B)(6) 2019. FURTHER INFORMATION REVEALED THAT THE PACKAGE WAS NOT VERIFIED PRIOR TO SURGERY. THERE HAS BEEN NO PATIENT INJURY OR IMPACT REPORTED, HOWEVER THE PATIENT WILL CONTINUE TO BE MONITORED. THE SURGEON PLANS ON LEAVING THE IMPLANT IN THE PATIENT. THIS REPORT IS BEING RAISED AS A DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8632594 ↗
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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