Devicor Medical Products Inc: Medical Device Recall in 2020 - (Recall #: Z-0070-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Neoprobe GDS Control Unit, Model Number NPCU3

Product Classification:

Class III

Date Initiated: September 7, 2020

Date Posted: October 14, 2020

Recall Number: Z-0070-2021

Event ID: 86228

Reason for Recall:

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.

Status: Terminated

Product Quantity: 49

Code Information:

UDI: 00841911100317; Serial Numbers: 122066557 122066558 122066559 122066560 122066561 122666652 123066667 123066668 123066669 123366695 123366696 123366697 123366698 123366699 123366700 123366701 123366702 123266693 123266694 134467282 143367591 144867780 145067796 150367828 150367829 150367840 150467866 150467867 150367830 150367831 150367832 150967913 150967914 151067915 151067916 151067917 151267970 151267971 151267972 151267973 151267974 185269399 185269403 190269421 190469433 190469430 190469428 150467871 150467869

Distribution Pattern:

The products were distributed only to China.

Voluntary or Mandated:

Voluntary: Firm initiated