RegWardenFDA facility compliance records
Recall

Class II — Novarad Corporation

Recalling firmNOVARAD CORP.
Registered facilityNOVARAD CORP. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonNovarad Corporation announces a voluntary field action for the NovaPACS versions 8.4.7, 8.5.3, and 8.5.6 due to a "pop-up screen" that was prematurely released.
ProductNovaPACS versions 8.4.7, 8.5.3, and 8.5.6. Distributed by Novarad Corporation. Picture archiving and communication system (PACS) Product Usage NovaPACS is a picture archiving and communication system software that retrieves, archives, distributes, and displays images and data from all common modalities. NovaPACS uses a variety of workstations, including a Technologist Workstation, Enterprise Radiologist Workstation, Cardio Viewer and Workstation, NovaMG Workstation, and NovaWeb Web Viewer. The NovaPACS software makes images and data available in digital format from all common modalities. The…
Quantity90
DistributionWorldwide Distribution - US (Nationwide) Canada and other foreign consignees.
Initiated2016-08-12
Classified2016-08-25
Terminated2017-02-22
Recall numberZ-2659-2016
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Novarad Corporation (Z-2659-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74937/

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