FDA Recall Open, Classified

GM60A. Digital Diagnostic Mobile X-Ray System.

Recall: Z-2715-2024 · Initiated July 8, 2024

Recall

Recall Number
Z-2715-2024
Event Number
95100
Firm
NeuroLogica Corporation
FEI Number
3004938766
Product Code
IZL
Status
Open, Classified
Root Cause
Device Design
Initiated
July 8, 2024
Posted
August 22, 2024
Address
14 Electronics Ave, Danvers, MA, 01923-1011

Description

GM60A. Digital Diagnostic Mobile X-Ray System.

Reason

Potential for the anti-fall system of the device arm to fail.

Action

Consignees were emailed an "Urgent -- Medical Device Correction; GM60A Digital X-ray Imaging System" notification the week of 7/8/2024. The notification instructs consignees to share the recall notification with those in their organization that utilize the affected devices and forward the notification if devices have been transferred. Affected systems may continue to be used. Consignees are to check on-hand devices to confirm if they are affected by the field action and return the response form back indicating any devices that require correction by email to [email protected] within 10 business days. Samsung Electronics will send service engineers to affected consignees to correct devices free of charge. Service will be coordinated by Samsung Electronics and should be completed by October 2024. Consignees with any questions are to contact their local Samsung Electronics representative.

Distribution

US Nationwide distribution in the states of AR, CT, GA, IN, KS, MA, MD, MO, MS, NC, ND, NJ, NV, OH, PA, VA, WV & DC.

Quantity

31 units