NovaSignal Corp.: Device Recall
Recall #Z-2216-2024 · 05/06/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2216-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- NovaSignal Corp.
- Status
- Ongoing
- Date Initiated
- 05/06/2024
- Location
- Los Angeles, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 45 systems
Reason for Recall
Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.
Product Description
NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA
Distribution Pattern
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.
Other Recalls by NovaSignal Corp.
- Class II: Risk 05/06/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.