TriMark TRIMARKTD-2S-13-MRRecalls & reported problems

Hologic, Inc. · TriMark TrapDoor (TD) · Class 2 · Implant

All models of TriMark (9)

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 05420045503345), received between May 15, 2025 and May 15, 2025 — 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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Adverse Event Without Identified Device or Use Problem1

Patient problems

Foreign Body In Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryMay 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DURING AN ATEC PROCEDURE ON (B)(6) 2025, AN ARTIFACT WAS OBSERVED IN THE PATIENT'S BREAST AFTER AN MRI BIOPSY IN ADDITION TO THE TRIMARKTD-2S-13-MR MARKER THAT WAS DEPLOYED AT THE TIME. IT IS REPORTED THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY; HOWEVER, THE CUSTOMER REPORTS THAT THE PATIENT REQUIRED ADDITIONAL MEDICAL OR SURGICAL INTERVENTION. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Foreign Body In Patient
MAUDE report 22031090 ↗

Device details

UDI-DI	`05420045503345`
Brand	TriMark
Model	TRIMARKTD-2S-13-MR
Company	Hologic, Inc.
Product code	NEU · MARKER, RADIOGRAPHIC, IMPLANTABLE
Class	Class 2
FDA submission	K023450
Implant	Yes
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	MR Conditional
Status	In Commercial Distribution
Record updated	Apr 8, 2024

Device type (GMDN): Radiological image marker, implantable

A device intended to be implanted within the body, either temporarily or permanently, to create identifying marks that can be seen on radiographic film or digital images. It is typically in the form of a wire, needle, bead, clip, stent-like tube, washer or fluid, and used to locate and delineate a tumour, lesion, or other site of interest. It is made from materials compatible with the imaging system with which it is intended to be used [e.g., magnetic resonance imaging (MRI), x-ray, or nuclear medicine]; it may be intended for use during radiotherapy procedures.

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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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