Arsenal Foot 300-88-001Recalls & reported problems
Trilliant Surgical, LLC · Arsenal L Plate, Left · 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 00810028390270), received between Jun 15, 2021 and Jun 15, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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
- Migration1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 15, 2021Migration; Migration
ON (B)(6) 2021, A TRILLIANT SURGICAL INDEPENDENT SALES REPRESENTATIVE EMAILED TWO (2) DJO FOOT & ANKLE SALES SUPPORT SPECIALISTS TO REPORT A REMOVAL OF A 300-88-001 (ARSENAL L PLATE, LEFT) AND ASSOCIATED CONSTRUCT ON (B)(6) 2021 BY DOCTOR 1 AT FACILITY 1 ON A (B)(6) FEMALE PATIENT DUE TO REPORTED PATIENT PAIN AT THE SURGICAL SITE AS A SCREW "BACKED OUT". THE CONSTRUCT IMPLANTATION OCCURRED ON (B)(6) 2021 BY DOCTOR 1 AT FACILITY 1 AND INCLUDED THE 300-88-001 (ARSENAL L PLATE, LEFT), 308-27-026 (2.7MM X 26MM ARSENAL LOCKING SCREW), 307-27-024 (2.7MM X 24MM ARSENAL SCREW), AND 308-27-022 (2.7MM X 22MM ARSENAL LOCKING SCREW). IT WAS REPORTED THAT THE PATIENT WAS NON-COMPLIANT AS SHE BEGAN WALKING TOO SOON AFTER THE IMPLANTATION. THE ENTIRE CONSTRUCT WAS RETAINED BY THE FACILITY AND WILL NOT BE RETURNED TO CORPORATE FOR FURTHER REVIEW.
Patient problems: Pain
MAUDE report 12001873 ↗
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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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