Devicor Medical Products recalls

Recall found. Devicor Medical Products is named in FDA Class II recall Z-2239-2026 covering HydroMARK Breast Biopsy Site Marker. Hazard: Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers. Identifying details: Lot Number: F12607207D. Status: Ongoing.

Models with recalls

HydroMARK Breast Biopsy Site Marker (1)

All Devicor Medical Products recalls

FDA Class II · Medical device · June 3, 2026

HydroMARK Breast Biopsy Site Marker recall — Devicor Medical Products Inc

Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.

Official ID Z-2239-2026 · Official record ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.