FDA Recall Terminated

The GC80 Digital X-ray Imaging System

Recall: Z-0726-2018 · Initiated June 22, 2017

Recall

Recall Number
Z-0726-2018
Event Number
78679
Firm
NeuroLogica Corporation
FEI Number
3004938766
Product Code
KPR
Status
Terminated
Root Cause
Other
Initiated
June 22, 2017
Terminated
October 5, 2018
Address
14 Electronics Ave, Danvers, MA, 01923-1011

Description

The GC80 Digital X-ray Imaging System

Reason

An image was obtained with over exposure during a Thorax examination using the AEC function.

Action

On June 22, 2017, Samsung distributed Urgent Field Safety Notices & acknowledgment forms to their customers via email. INSTRUCTIONS FOR END USERS: 1) Please read the Field Safety Notice documentation in detail. 2) Follow the instructions provided in this FSN in relation to any actions which are required of you. 3) Complete the provided acknowledgement form and return to your supplier as soon as possible. Your organizations reply is the evidence we need to monitor the progress of the corrective actions. 4) If required and instructed by this FSN documentation, please undertake all relevant service actions as soon as is practicably possible. INSTRUCTIONS FOR DISTRIBUTORS: 1) Please read the Field Safety Notice documentation in detail. 2) Please review and complete the acknowledgement form provided in this FSN and return to Samsung as soon as possible. Please pass this entire package of FSN documentation onto your customers and ask them to return the completed acknowledgement form. Please forward copies of acknowledgements from end users onto to the email addresses stated above. Samsung require this evidence to monitor the progress of the corrective actions. 4) If required and instructed by this FSN documentation, please undertake all relevant service actions as soon as is practicably possible. Customers with questions were advised to contact their local representative.

Distribution

Nationwide US

Quantity

45 units