Luminos Agile Max, model no. 10762471 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal, thoracic and lung exposures as well as examinations of the urogenital tract.
FDA Recall Z-1338-2020 · Posted None
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Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeOWB
Date Initiated2020-01-08
Date Terminated2022-06-21
Product Quantity475
Reason for Recall
A software bug may lead to one image to be assigned to two different patients, which could potentially affect medical diagnosis.
Firm Action
On January 8, 2020, the firm notified customers of the product issue via an Urgent Medical Device Correction letter.
Customers were instructed to ensure that the image displayed after acquisition is a newly acquired image and belongs to the current patient. If the error occurs and a previously acquired image is duplicated, the user should delete the image and contact Siemens
Customer Service at 1-800-888-7436 to report the incident.
Siemens Healthineers will correct the error with a field software update which will be available beginning January 2020. Your local Siemens Healthineers Service organization will contact you to arrange a date to perform this
corrective action when the software update is available for your system. Please feel free to contact our service
organization for an earlier appointment at 1-800-888-7436.
Root Cause
Software design
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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