FDA recall record

Novarad NovaPACS  Diagnostic Viewer versions 8.3.7, 8.4.2, 8.4.3, and 8.4.4 recall — FDA Z-1613-2016

The SUV values that are being calculated in the PET/CT fusion tool are incorrect.

Class IIclassification
Z-1613-2016official record ID
May 18, 2016report date

Recall record at a glance

Official recordZ-1613-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNovarad Corporation
Report dateMay 18, 2016
Recall initiation dateNov 16, 2015
Quantity2,386
LocationAmerican Fork, UT, United States

Official product description

NovaPACS  Diagnostic Viewer versions 8.3.7, 8.4.2, 8.4.3, and 8.4.4. Novarad Corporation

Why the product was recalled

The SUV values that are being calculated in the PET/CT fusion tool are incorrect.

Distribution information

Nationwide. 3 Canadian and 33 foreign consignees. No VA/gov/military.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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Related recall records

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Novarad NovaPACS Diagnostic Viewer recall — FDA Z-2956-2020

The firm received a report of an atypical dataset being generated. When using the cross-localization feature and images from a modality that generates asymmetrical images, the…

Class IIFDA: TerminatedNovarad Corporation