NA 0407281000Recalls & reported problems
Stryker Corporation · Percutaneous Discectomy Probe · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540500229), received between Nov 14, 2018 and Dec 17, 2021 — classified as 1 injury, 1 malfunction.
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
- Fracture1
Patient problems
- Device Embedded In Tissue or Plaque1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 17, 2021Fracture; Fracture
THE USER FACILITY REPORTED, THE DEVICE AND NEEDLE BROKE OFF DURING PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO SIGNIFICANT SURGERY DELAY, NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED AS RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13027469 ↗InjuryNov 14, 2018Break; Break
IT WAS REPORTED THAT DURING A PROCEDURE, THE PROBE BROKE OFF INSIDE OF THE PATIENT. THE PROCEDURE WAS NOT SUCCESSFULLY COMPLETED AS MEDICAL INTERVENTION WAS NECESSARY TO REMOVE THE DEVICE MATERIAL. NO ADDITIONAL ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 8071656 ↗
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- MITEK 242018Medos International Sàrl · Arthroscope731 reports
- METRx® System 9560100Medtronic Sofamor Danek, Inc. · Arthroscope667 reports
- FMS VUE II 284004Medos International Sàrl · Arthroscope562 reports
- VAPR COOLPULSE 228146Depuy Mitek, LLC · ARTHROSCOPE474 reports
- FMS DUO 284580Depuy Mitek, LLC · ARTHROSCOPE458 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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