Devicor Medical Products recalls
Devicor Medical Products has 5 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 3 Jun 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is sterility.
Total recalls5since 2016
Last 12 months1reported
Class I00% of total
Ongoing1latest 3 Jun 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 80%Class III 1 20%
Why devicor medical products is recalled
Product types
By year
Ongoing devicor medical products recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | HydroMARK Breast Biopsy Site Marker recalled by Devicor Medical Products | Devicor Medical Products | Packaging Defects | Nationwide |
All devicor medical products recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | HydroMARK Breast Biopsy Site Marker recalled by Devicor Medical Products | Devicor Medical Products | Packaging Defects | Nationwide |
| Device | CLASS II | HydroMARK Breast Biopsy Marker recalled by Devicor Medical Products | Devicor Medical Products | Other | Nationwide |
| Device | CLASS III | Neoprobe GDS Control Unit recalled by Devicor Medical Products | Devicor Medical Products | Device Malfunction | OH |
| Device | CLASS II | Mammotome Revolve Dual Vacuum Assist Biopsy System recalled | Devicor Medical Products | Sterility | Nationwide |
| Device | CLASS II | Mammotome Revolve Dual Vacuum Assist Biopsy System recalled | Devicor Medical Products | Sterility | 26 states |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.