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Devicor Medical Products Recalls
5 recalls on record · July 20, 2016 to June 3, 2026 · Medical Devices
Recalls by year
16
17
20
22
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 3, 2026Medical DevicesFDA
Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
Hazard: Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.
June 1, 2022Medical DevicesFDA
Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
Hazard: Small patient labels do not match the primary device label. The primary device label accurately identifies the product as 4010-05-08-T4, while the smaller patient label incorrectly identifies the product as 4010-05-08-T3.
October 14, 2020Medical DevicesFDA
Devicor Medical Products Inc recalls Neoprobe GDS Control Unit, Model Number NPCU3
Hazard: It was discovered during a documentation review that China has the software version as v5.01 approved for use in China. The current software version on devices distributed in China since 2011 is v6.01.
March 29, 2017Medical DevicesFDA
Devicor Medical Products Inc recalls Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identifie
Hazard: The device did not have Revolve Stereo Probe labeling, no product code indicating the size and length of the probe, no sterilization sticker or lot number.
July 20, 2016Medical DevicesFDA
Devicor Medical Products Inc recalls Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged w
Hazard: A 10 Gauge needle, 9cm long was shipped in an 8 Gauge needle, 15 cm package.