Arsenal Foot 300-83-002Recalls & reported problems
Trilliant Surgical, LLC · Arsenal Petite Lapidus Plate, R · 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 00810028390157), received between Apr 3, 2020 and Apr 3, 2020 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Erosion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 3, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON (B)(6) 2020, A TRILLIANT SURGICAL SALES REPRESENTATIVE CALLED IN TO REPORT THE REMOVAL OF A ARSENAL PETITE LAPIDUS PLATE, R (300-83-002) AND ITS ASSOCIATED IMPLANTED ARSENAL SCREWS (REFERENCE DIAMETERS AND LENGTHS BELOW). THE DATE OF IMPLANTATION WAS (B)(6) 2019, PERFORMED BY DOCTOR 1 AT FACILITY (B)(6) ON AN (B)(6) YEAR OLD, (B)(6) POUND, FEMALE PATIENT. THE SALES REPRESENTATIVE REPORTED THAT DOCTOR 1 SAW THE PATIENT IN-OFFICE ON (B)(6) 2020. AT THAT TIME, DOCTOR 1 NOTICED A SCAB ON THE PATIENT'S RIGHT GREATER TOE DEVELOPED INTO A WOUND. SURGICAL INTERVENTION WAS SCHEDULED FOR (B)(6) 2020 AT FACILITY X TO REMOVE THE LAPIDUS PLATING CONSTRUCT, WHICH IS THE DATE THE SALES REPRESENTATIVE WAS NOTIFIED OF THE REMOVAL. UPON CT EVALUATION, DOCTOR 1 DETERMINED UNION OF THE GREAT TOE HAD ALMOST COMPLETELY FORMED. IN ORDER TO ENSURE 100% UNION, DOCTOR 1 LEFT THE INTERFRAGMENTARY 4.5MM X 45MM HEADLESS, STTHCS (202-45-045) IMPLANTED AND ONLY REMOVED THE IMPLANTED 300-83-002 AND ASSOCIATED IMPLANTED ARSENAL SCREWS. THE 300-83-002 PLATE AND ASSOCIATED ARSENAL SCREWS WERE RETURNED BY THE SALES REPRESENTATIVE TO TRILLIANT SURGICAL'S CORPORATE OFFICE FOR FURTHER REVIEW. ALL DISCUSSED PARTS WERE
Patient problems: Erosion
MAUDE report 9921888 ↗
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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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