Tornier Perform MWJ124Recalls & reported problems
Tornier, Inc. · Peripheral Screw Drill Guide · Class 1
- 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 00846832062478), received between Dec 12, 2023 and Dec 12, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Residue After Decontamination” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Residue After Decontamination1
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.
InjuryDec 12, 2023Residue After Decontamination; Residue After Decontamination
AS REPORTED: "THE SCRUB COULD NOT GET THE DISPOSABLE DRILL BIT THROUGH THE PERIPHERAL DRILL GUIDE MWJ124. AFTER PUSHING THROUGH A LOT OF BLACK DIRT (OLD BLOOD) CAME OUT AND WAS SPREAD OVER THE TRAY. WE WERE FORCED TO MOVE TO REV II WITH BIO RSA. PATIENT GOT A DIFFERENT GLENOID OPTION THAN DISCUSSED. SURGEON WAS FORCED TO MOVE TO DIFFERENT GLENOID OPTION." UPDATE: REVERSED II OPTION WAS INDEED SUCCESSFUL TO COMPLETE THE SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18314447 ↗
Other Guide, surgical, instrument devices
- NA 03.037.017Synthes GmbH · Guide, surgical, instrument346 reports
- EVOS 71174934Smith & Nephew, Inc. · Guide, surgical, instrument149 reports
- LCP 323.042Synthes GmbH · Guide, surgical, instrument129 reports
- DJO SURGICAL 342-10-705Encore Medical, L.P. · Guide, Surgical, Instrument1 recall51 reports
- DJO SURGICAL 341-10-707Encore Medical, L.P. · Guide, Surgical, Instrument81 reports
- NA 03.010.404Synthes GmbH · Guide, surgical, instrument73 reports
- DJO SURGICAL 341-14-708Encore Medical, L.P. · Guide, Surgical, Instrument1 recall22 reports
- DJO SURGICAL 341-10-711Encore Medical, L.P. · Guide, Surgical, Instrument1 recall16 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.