FDAClass IIJuly 8, 2015

The VariSource iX series afterloader systems are recall

The VariSource iX series afterloader systems are computer controlled remote electro/mechanical systems used for medical purposes, for placing a cable…

Why was The VariSource iX series afterloader systems are recalled?

After an application freeze and restart of the VariSource iX series by power cycling, the Partial Fraction generated by the system will not be correct. The application freeze issue affects only the systems equipped with magnetic Hard Disk Drives (HDD).

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

JAQ

Product
The VariSource iX series afterloader systems are computer controlled remote electro/mechanical systems used for medical purposes, for placing a cable…
Recalling firm
Varian Medical Systems Inc
Quantity
55
Distribution
Worldwide Distribution.
Recall date
July 8, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
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