company
Devicor Medical Products Inc
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-03Devicor Medical Products Inc — Class II recall: HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
Frequently asked questions
- How many FDA warning letters has Devicor Medical Products Inc received?
- Argus HQ has not recorded an FDA warning letter for Devicor Medical Products Inc in our current dataset.
- What FDA recalls has Devicor Medical Products Inc issued?
- Argus HQ has recorded 1 FDA recall tied to Devicor Medical Products Inc.
- Is Devicor Medical Products Inc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Devicor Medical Products Inc. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.

