FDAClass IIJuly 3, 2024

NovaGuide 2 Traditional Ultrasound recall

NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2

Why was NovaGuide 2 Traditional Ultrasound recalled?

Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

UDI: 00850681007405/Serial Numbers: 21092746 21122802 21122803 21092748 21092749 21122804 21123066 23063826 22074381 23063828 22033706 22064206 22074380 21092747 22113115 23063825 21122805 21082646 23063856 23104174 21123068 22103022 22064204 22064205 21123067 22074378 22074379 23033578

Product
NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2
Recalling firm
NovaSignal Corp.
Quantity
28 systems
Distribution
Worldwide - US Nationwide distribution in the states of MA, TX, NY, MN, AZ, AL, CO, CA, OH, MO, FL, TN, NJ, GA, OK, KY, WA and the country of Canada.
Recall date
July 3, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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