FERKEL 72202154Recalls & reported problems
Smith & Nephew, Inc. · FERKEL MICROFRACTURE PICK 65 DEGREE · Class 1
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 03596010622334), received between Oct 6, 2021 and Oct 6, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 6, 2021Break; Break
IT WAS REPORTED THAT A MTO FERKEL MICROFRACTURE PICK 65 WAS PUT INTO THE ANKLE FOR A MICRO FRACTURE, BONE WAS SOFT, SO IT WAS EASILY INTRODUCED WITH MINIMAL FORCE (NO HAMMER NEEDED). ON REMOVAL FROM BONE THE TIP OF THE DEVICE BROKE OFF INSIDE OF THE PATIENT. ALL PIECES WERE RECOVERED REQUIRING EXTRA INCISIONS AND X-RAYS. PROCEDURE WAS COMPLETED USING A BACK-UP DEVICE. A SIGNIFICANT DELAY (GREATER THAN 30MIN) WAS REPORTED. NO OTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12583784 ↗
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- FirstPass 72290129Smith & Nephew, Inc. · Accessories, arthroscopic82 reports
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- MITEK 242025Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC61 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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