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Terminated

Varian High Energy Linear Accelerator: Varian Medical Systems, Palo Alto, CA 94304 Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.

FDA Recall Z-1045-2011 · Posted 2011-02-08

Recall StatusTerminated
Product CodeIYE
Date Initiated2010-12-10
Date Terminated2011-08-02
Product Quantity1882

Reason for Recall

An anomaly was identified whereby the bolts used to fasten the counterweight to the gantry may not, in some cases, be fully tightened to the required torque specification.

Firm Action

An Urgent Medical Device Correction letter was sent to all affected users with a description of the problem and user corrective action steps. Letters were sent on 12/10/2010. Users are to immediately investigate any unusual noises coming from the affected product and report them to whoever is responsible for servicing the device. For customers that do have a service contract with Varian, Varian service will perform an inspection of the counterweight bolts as part of the regular Periodic Maintenance Inspection procedure. Customers are to advice the appropriate personnel of the contents of the letter. For further clarification, customers can contact their local Varian Customer Support Services Manager.

Root Cause

Process control

Distribution Pattern

Worldwide 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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