Recall StatusTerminated
Date Initiated2020-07-15
Date Terminated2021-07-13
Product Quantity35
Reason for Recall
There are potential issues related to the operational state of the scanner, specifically for transport and inadvertent system shutdowns. There could be a possibility of potential delay in patient treatment if proper use instructions are not followed.
Firm Action
Urgent Medical Device Correction notification letters were sent to customers beginning 7/15/20.
Users may continue to use the NL5000 system if proper instructions for use are followed as described in user manual (1-NL5000-060).
This notice needs to be passed on all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred.
Please transfer this notice to other organizations on which this action has an impact. Please maintain awareness on this notice and resulting action for an appropriate period to ensure effectiveness of the corrective action.
The system label is located near the main input plug or on the side of the system.
NeuroLogica will undertake the voluntary corrective action considering the possibility of delay in patient treatment if the scanner is not operational. The hardware and software upgrades provide additional safeguards by improving the design to minimize any risks of the above situations from happening.
Service engineers will correct all affected devices free of charge and contact you to arrange for the correction. All corrections in the field will be completed by December 31, 2020.
If you need any further information or have any concerns with this issue, then please contact your local representative.
Customer Reply Form
This reply form is to confirm receipt of the enclosed NeuroLogica Medical Device Field Safety Notice [FSN-NL5000_071620] regarding the potential issues related to the operational state of the scanner and the required software and hardware upgrades. Please read the Notice and indicate the appropriate answers to the questions below.
Distribution Pattern
Worldwide distribution - US Nationwide distribution and the countries of Canada, India, Portugal, Singapore, Slovak Republic, Thailand, Turkey, UK.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.