INBONE 200380001Recalls & reported problems
Wright Medical Technology, Inc. · Wrench, TIB Stem · Class 1
All models of INBONE (56)
Data updated Oct 18, 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 00889797030915), received between Feb 17, 2026 and Feb 17, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Device Handling 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Handling Problem1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 17, 2026Device Handling Problem
AS REPORTED: "THE PRODUCT WAS THROWN AWAY IN THE TRASH BECAUSE THE REAMER HEAD PIECE 14MM (200046001) WAS BROKEN OFF ON THE REAMER ROD(200089). THE WRENCH SLID A LITTLE BIT AND BROKE THE MEDIAL MAL OR DISTAL TIBIA AND WE HAD TO FIX THE DISTAL TIBIA WITH ORIF WITH A MEDIAL MAL PLATE. THE PRODUCT WAS THROWN AWAY IN THE TRASH BECAUSE THE REAMER HEAD PIECE 14MM (200046001) WAS BROKEN OFF ON THE REAMER ROD(200089). THE WRENCH SLID A LITTLE BIT AND BROKE THE MEDIAL MAL OR DISTAL TIBIA AND WE HAD TO FIX THE DISTAL TIBIA WITH ORIF WITH A MEDIAL MAL PLATE".
Patient problems: Bone Fracture(s)
MAUDE report 24372787 ↗
Other WRENCH devices
- MONARCH 277040510Medos International Sàrl · WRENCH199 reports
- PINNACLE 2217-50-008Depuy (Ireland) · WRENCH108 reports
- SIGMA 96-1673Depuy (Ireland) · WRENCH102 reports
- P.F.C. 86-5189Depuy (Ireland) · WRENCH92 reports
- Veptr 03.641.004Synthes GmbH · WRENCH86 reports
- RECLAIM 2975-00-300Depuy (Ireland) · WRENCH51 reports
- PINNACLE 2217-50-006Depuy (Ireland) · WRENCH34 reports
- NA 388.261Synthes GmbH · WRENCH32 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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