Arsenal Foot 300-82-001Recalls & reported problems
Trilliant Surgical, LLC · Arsenal Petite MPJ Plate, L · Class 2 · Implant
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 00810028390089), received between Jul 15, 2021 and Jul 15, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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.
Most reported problems
Device problems
- Fracture1
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.
InjuryJul 15, 2021Fracture; Fracture
ON 06/17/2021, A TRILLIANT SURGICAL INDEPENDENT SALES REPRESENTATIVE CALLED A DJO FOOT & ANKLE SALES SUPPORT REPRESENTATIVE TO REPORT AN UPCOMING REMOVAL SURGERY OF A 300-82-001 (ARSENAL PETITE MPJ PLATE, L) AND ASSOCIATED SCREWS BY DOCTOR 1 AT FACILITY 1. THE ORIGINAL IMPLANT SURGERY WAS AN MPJ FUSION WHICH TOOK PLACE ON (B)(6) 2021 AT FACILITY 1 ON A (B)(6) YEAR-OLD NEUROPATHIC FEMALE PATIENT WHO HAS A HISTORY OF PREVIOUS AILMENTS AND PROCEDURES TO THE LEFT FOOT. DOCTOR 1 STATED THAT THE 300-82-001 HAS BROKEN, AND ON (B)(6) 2021, HE WILL REMOVE THE ENTIRE CONSTRUCT: ONE (1) 300-82-001 (ARSENAL PETITE MPJ PLATE, L), ONE (1) 307-27-018 (2.7MM X 18MM ARSENAL SCREW), ONE (1) 308-27-008 (2.7MM X 8MM ARSENAL LOCKING SCREW), TWO (2) 308-27-012 (2.7MM X 12MM ARSENAL LOCKING SCREW), TWO (2) 308-27-016 (2.7MM X 16MM ARSENAL LOCKING SCREW), AND ONE (1) 200-30-026 (3.0MM X 26MM TIGER CANNULATED SCREW). DOCTOR 1 PLANS TO IMPLANT A REVISIONAL CONSTRUCT. DOCTOR 1 BELIEVES THE PATIENT TO HAVE BEEN COMPLIANT UNTIL THE PLATE BROKE ABOUT 11 WEEKS AFTER THE IMPLANT SURGERY, BUT WILL WORK TO OBTAIN MORE DETAILS FROM THE PATIENT PRIOR TO THE REMOVAL SURGERY. X-RAYS WERE PROVIDED BY THE FACILITY OF THE
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12177425 ↗
Other Plate, Fixation, Bone devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page