FDA recall record

Varian Medical Systems Optical Surface Monitoring System{OSMS, Varian Private Label} This is recall — FDA Z-2149-2016

Varian Medical Systems has received reports that unintended changes were made to planned couch parameters, specifically the couch rotation parameter,…

Class IIclassification
Z-2149-2016official record ID
Jul 20, 2016report date

Recall record at a glance

Official recordZ-2149-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmVarian Medical Systems, Inc.
Report dateJul 20, 2016
Recall initiation dateJun 23, 2016
Quantity166 OSMS in US, 23 OSMO - International,
LocationPalo Alto, CA, United States

Official product description

Optical Surface Monitoring System{OSMS, Varian Private Label} This is used on Varian's TrueBeam EDGE; Radiology: The AlignRT Plus system is indicated for use to position and monitor patients relative to the prescribed treatment isocentre, and to Withhold the beam automatically during radiation delivery.

Why the product was recalled

Varian Medical Systems has received reports that unintended changes were made to planned couch parameters, specifically the couch rotation parameter, during patient set-up. This can occur when a user sets a different couch rotation from the plan couch rotation while performing patient alignment with Optical Surface Monitoring System [OSMS].

Distribution information

Worldwide Distribution: US (nationwide) and countries of: Austria, Azerbaijan, Brunei Darussalam, Bulgaria, Denmark, Georgia, Germany, India, Italy, Malaysia, Morocco, Norway, Portugal, Switzerland, and United Kingdom.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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