NeuroLogica Corporation: Device Recall
Recall #Z-2715-2024 · 07/08/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2715-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- NeuroLogica Corporation
- Status
- Ongoing
- Date Initiated
- 07/08/2024
- Location
- Danvers, MA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 31 units
Reason for Recall
Potential for the anti-fall system of the device arm to fail.
Product Description
GM60A. Digital Diagnostic Mobile X-Ray System.
Distribution Pattern
US Nationwide distribution in the states of AR, CT, GA, IN, KS, MA, MD, MO, MS, NC, ND, NJ, NV, OH, PA, VA, WV & DC.
Other Recalls by NeuroLogica Corporation
- Class II: Risk 10/07/2025
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.