Drug recall
HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
FDA recall event 98843 · Class II · Devicor Medical Products Inc
Key facts
| Event ID | 98843 |
|---|---|
| Recall numbers | Z-2239-2026 |
| Recalling firm | Devicor Medical Products Inc |
| Product type | Devices |
| Products | HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers. |
| Initiation date | Apr 24, 2026 |
| Report date | Jun 3, 2026 |
| City | Cincinnati |
| State | OH |
| Country | United States |
| FEI number | 3008492462 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: