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U.S. Department of Health and Human Services

Class 2 Device Recall INTIO Inc. ClearStartSVM

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 Class 2 Device Recall INTIO Inc. ClearStartSVMsee related information
Date Initiated by FirmFebruary 26, 2013
Date PostedMarch 20, 2013
Recall Status1 Terminated 3 on April 17, 2013
Recall NumberZ-0974-2013
Recall Event ID 64435
510(K)NumberK113541 
Product Classification System, image processing, radiological - Product Code LLZ
ProductINTIO Inc., ClearStart-SVM Segmentation and Volumetric Measurement System, Users Manual. Part #: UM-06-20-0003. ClearStart-SVM is used for patient assessment using CT (computed tomography) images, in order to plan potential therapies or monitor tumor response to treatment.
Code Information INTIO Inc. Part #: UM-06-20-0003 for SVM User's Manual
Recalling Firm/
Manufacturer		 Intio Inc
325 Interlocken Pkwy
Broomfield CO 80021-3497
For Additional Information ContactAlf Granger
303-396-0291
Manufacturer Reason
for Recall		INTIO Inc. distributed a SVM User's Manual and it has an editing mistake that could be interpreted as promoting an unapproved use.
FDA Determined
Cause 2		Labeling False and Misleading
ActionINTIO sent a Recall Notice to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. INTIO has corrected this version of the SVM User's Manual. An INTIO Inc. employee will contact the customers to replace the current manual with the correct one. Consignees were notified by letter that an INTIO Inc. employee will contact you within the next 30 days to replace the current manual with the correct one. The new SVM User's Manual will be provided to you once INTIO Inc. has retrieved the incorrect version of the SVM User's Manual. Customers with questions were instructed to email support@intio.us or call 303-396-1777. For questions regarding this recall call 303-396-9291.
Quantity in Commerce7
DistributionNationwide Distribution including MN, FL, PA, WI, NY, and RI.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = LLZ
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