Iconix 3911-714-571Recalls & reported problems
Riverpoint Medical, LLC · Iconix Hard Bone Drill for 1.4mm Iconix Knotless. · Class 1
All models of Iconix (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00840277402592), received between Oct 22, 2025 and May 28, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Integrity Problem” (3 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.
Reports received per month
Most reported problems
Device problems
- Material Integrity Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 28, 2026Material Integrity Problem
ACCORDING TO THE REPORTER, "SURGEON WAS ABOUT TO PUT THE FIRST ANCHOR IN THE PATIENT AND THE PA DID THE DRILLING, BIG PART OF THE TIP OF THE DRILL BROKE INSIDE THE PATIENT AND COULDN'T TAKE IT OUT. AFTER THE FIRST ANCHOR COMPLETELY PULLED OUT AFTER INSERTING IT, WE TRIED DRILLING IN ANOTHER SPOT THAT HAD BETTER BONE. I NOTICED THAT THE DRILL WENT STRAIGHT IN AND OUT WITHOUT ANY RESISTANCE SO THE TECH TOOK OUT THE DRILL AND NOTICED THE TIP WAS CLEARLY SNAPPED OFF. WE TOOK AN XRAY AFTER TO SEE IF IT WAS INSIDE THE PATIENT AND IT WAS. WE TRIED SEEING IF WE COULD FIND A TIP TO MAYBE REMOVE IT BUT IT ENDED UP BEING BURIED IN BONE SO STAYED THERE. SURGEON WAS VERY UPSET AND JUST ENDED UP PUTTING IN ANOTHER ANCHOR INSTEAD OF 2 MORE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25325582 ↗MalfunctionMar 16, 2026Material Integrity Problem
ACCORDING TO THE REPORTER: " 1.4MM HARD BONE DRILL BIT, BROKE OFF INSIDE THE ACETABULAR RIM DURING A HIP ARTHROSCOPY SURGERY, SURGEON MADE THE DECISION TO LEAVE A BIT OF THE DRILL IN THE BONE TO NOT CAUSE MORE DAMAGE TO THE BONE. THE SURGEON STATED THE BONE WAS VERY HARD AND THAT IS WHY IT MOST LIKELY HAPPENED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24611799 ↗MalfunctionOct 22, 2025Material Integrity Problem; Material Integrity Problem
ACCORDING TO THE REPORTER, "THIS CASE WITH DR.(B)(6). HE ATTEMPTED TO USE AN ICONIX KNOTLESS ANCHOR WITH THE HARD BONE DRILL BIT AND IT WAS UNSUCCESSFUL AND ABORTED THE ANCHOR."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23360596 ↗
Other Bit, Drill devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 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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