Devicor Medical Products Inc recalls
Every recall we track for Devicor Medical Products Inc — 3 in all, from 2020–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Devicor Medical Products Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 1 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Devicor Medical Products Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Devicor Medical Products Inc recalls
3 shown- Lower riskMedical device
Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
Devicor Medical Products recalls HydroMARK Breast Biopsy Site Marker Model 4010-02-15-T3 due to incorrect inner package labeling. Boxes labeled 401:02:15-T3 may contain T4 markers instead.
Devicor Medical ProductsApr 24, 2026 - Lower riskMedical device
Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
Devicor recalls HydroMARK Breast Biopsy Marker Model 4010-05-08-T4 due to patient labels incorrectly identifying the product as a different model. This mismatch could lead to confusion during medical procedures.
Devicor Medical ProductsMar 30, 2022 - UnratedMedical device
Devicor Medical Products Inc recalls Neoprobe GDS Control Unit, Model Number NPCU3
Devicor Medical recalls Neoprobe GDS Control Units (Model NPCU3) with China-specific software version v6.01 that may not meet China's regulatory standards. Affected units were sold in China since 2011.
Devicor MedicalSep 7, 2020
Devicor Medical Products Inc recall questions
How many recalls has Devicor Medical Products Inc had?
3 recalls from Devicor Medical Products Inc are on record with U.S. safety agencies, from 2020–2026.
What is the most recent Devicor Medical Products Inc recall?
Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3, dated Apr 24, 2026. Every Devicor Medical Products Inc recall is listed on this page, newest first.
What should I do if I have a recalled Devicor Medical Products Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Devicor Medical Products Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.