FDA Recall Terminated

Neoprobe GDS Control Unit, Model Number NPCU3

Recall: Z-0070-2021 · Initiated September 7, 2020

Recall

Recall Number
Z-0070-2021
Event Number
86228
Firm
Devicor Medical Products Inc
FEI Number
3008492462
Product Code
IZD
Status
Terminated
Root Cause
Process design
Initiated
September 7, 2020
Terminated
May 9, 2023
Address
300 E Business Way, Fl 5, Cincinnati, OH, 45241-2384

Description

Neoprobe GDS Control Unit, Model Number NPCU3

Reason

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.

Action

URGENT FIELD CORRECTION notification letters were sent to customers. Action to be taken by the user: As a result of this notification, please conduct the following: " Please Examine your inventory, identify and reference attached product list to determine if you have an affected device. " If you have any Devices referenced, immediately contact Minghui Qian at +86 21 8031 6329 " If in use on a patient, continue to use the device if an alternative device is not available. " Please complete and return the enclosed Response Form of Acknowledgement. " If you have any additional questions, comments or concerns please contact our Customer Support at +86 21 8031 6329. You may also email [email protected].

Distribution

The products were distributed only to China.

Quantity

49