Arsenal Foot 300-84-001Recalls & reported problems
Trilliant Surgical, LLC · Arsenal 5th Met Hook 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 00810028390201), received between Oct 6, 2020 and Oct 6, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Positioning Failure” (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
- Positioning Failure1
Patient problems
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 6, 2020Positioning Failure; Positioning Failure
ON 09/08/2020, A TRILLIANT SURGICAL SALES REPRESENTATIVE REPORTED A REMOVAL OF AN IMPLANTED 300-84-001 (ARSENAL 5TH MET HOOK PLATE, L). THE REPORTED REMOVAL WAS PERFORMED BY DOCTOR 1 AT FACILITY X ON (B)(6) 2020, AFTER THE PATIENT REPORTED PAIN DURING A POSTOPERATIVE APPOINTMENT IN (B)(6) 2020. IT WAS LATER CONFIRMED THAT THE FIRST REPORT OF PAIN OCCURRED ON (B)(6) 2020. THE PATIENT WAS A (B)(6)-YEAR-OLD (DOB: (B)(6) 1970) FEMALE, (B)(6)POUNDS, WITH REPORTED GOOD BONE QUALITY. THE PATIENT DID NOT HAVE ANY REPORTED COMORBIDITIES, AND NO NON-COMPLIANCE WAS REPORTED. THE 300-84-001 WAS ORIGINALLY IMPLANTED ON (B)(6) 2020, AT FACILITY X BY DOCTOR 1. AT THE TIME OF IMPLANTATION, THE SALES REPRESENTATIVE REPORTED THAT DOCTOR 1 THOUGHT A REMOVAL PROCEDURE WOULD BE NEEDED DUE TO THE PLACEMENT OF THE PLATE. THE PLATES TINES WERE NOT FULLY INSERTED INTO THE BASE OF THE 5TH METATARSAL, MAKING IT SO THE PLATE WASN'T FLUSH AGAINST THE BASE. IN (B)(6) 2020, THE PATIENT REPORTED IN A POSTOPERATIVE APPOINTMENT THAT SHE WAS EXPERIENCING PAIN, UNKNOWN IF THE PAIN WAS LOCALIZED OR NOT. UNION OF THE FRACTURE IN THE 5TH METATARSAL WAS SEEN UPON X-RAY EXAMINATION. A REMOVAL PROCEDURE WAS SCHEDULED FOR (
Patient problems: Implant Pain
MAUDE report 10634948 ↗
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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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