Recall StatusTerminated
Date Initiated2020-10-19
Date Terminated2021-08-31
Product Quantity8 units
Reason for Recall
Treatment beam information disappears on Treatment Console screen while beam delivery continues potential for harm to a patient could occur
Firm Action
Mevion issued User Notice by mail or FedEx, with return receipt confirmation on October 22, 2020. The letter states reason for recall, health risk and action to take:
The User should actively monitor the TC screen during beam delivery. In the
event the TC screen beam information appears blank during Beam On, the user should:
Immediately suspend treatment by selecting Beam Off on the Beam
Control Box.
Record the MU counts displayed on the HMUC before any other action is
taken.
Consult physics to make manual adjustments of the plan.
Notify Field Service to retrieve machine records of the partial beam
delivery.
Resumption of treatment requires Setup workflow to be repeated.
Corrective Action
All users should be notified of this scenario and the proper response.
Please contact Mevion Customer service with any questions or concerns.
Please distribute this notice to all users of the Mevion Medical Systems device at your organization who may be affected by this issue
User confirmation of receipt shall also be received from each affected customer site. Customer Service Engineers are also permanently in working residence at customer sites and will ensure awareness of the issue.
Distribution Pattern
Worldwide distribution - US Nationwide distribution including in the states of DC, FL, MO, NJ, OK and the country of Netherlands.
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.