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Terminated

Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The GM85 Digital X-ray imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications

FDA Recall Z-1691-2019 · Posted None

Recall StatusTerminated
Product CodeIZL
Date Initiated2019-05-06
Date Terminated2020-06-10
Product Quantity288 systems

Reason for Recall

Potential issue related to the operation of the safety latch within the column that supports the arm due to a possibility of potential bodily harm due to a fall of the arm in an unlikely event that the column wire breaks.

Firm Action

NeuroLogica Corporation, a subsidiary of Samsung Electronics issued Medical Device Correction Notice on 05/06/19 advising users of the problem, health risk and action to take: 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 September, 2019. Users may continue to use the GM85 system. 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.If you need any further information or have any concerns with this issue then please contact your local representative

Root Cause

Process control

Distribution Pattern

US Nationwide Distribution

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.

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