ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in Radiation Therapy, Radiology, or Radiology image-guided treatment environment. Part Number: 1SOPT00003
FDA Recall Z-0398-2024 · Posted 2023-11-21
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Recalling FirmLEONI CIA CABLE SYSTEMS
Recall StatusOpen, Classified
Product CodeJAI
Date Initiated2023-10-06
Product Quantity1 unit
Reason for Recall
Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.
Firm Action
BizLink s notified customer via email with delivery and read confirmation and with the Field Safety Notice (FSCA Ref: UMCU-638) on October 6, 2023. Letter states reason for recall, health risk and action to take:
BizLink technical support team will contact customers shortly to organize the deployment of the hot fix in the proton-therapy treatment centers.
While waiting for the hot fix, BizLink recommend that customers implement the following action at the customer software level to avoid this problem:
Send a stopFast command just after reactivating the motionEnable / the E-stop / the collision detection by Safety Laser and before sending any other motion command.
A hot fix to correct this bug has been developed.
BizLink shall provide this hot fix (version OSS 6.1 and version OSS 7.3) and the detailed documentation so that customers can deploy the new software version on clinical sites
available on October 27, 2023 at the latest.
If you require further clarification, please feel free to contact our BizLink Team ([email protected]).
Please return the signed copy of the FSN to BizLink ([email protected]) within 10 working days
Root Cause
Software design
Distribution Pattern
US Nationwide distribution in the states of MA, TN.
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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