Klinika Mdical Gmb: Device Recall
Recall #Z-1769-2025 · 04/04/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1769-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Klinika Mdical Gmb
- Status
- Ongoing
- Date Initiated
- 04/04/2025
- Location
- Usingen, Germany
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 160 units
Reason for Recall
Potential for microbial contamination.
Product Description
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and positioning of tissue to be removed in the patient's body, enabling improved surgical precision and patient safety.
Distribution Pattern
US Nationwide distribution in the state of Massachusetts.
Other Recalls by Klinika Mdical Gmb
- Class II: Risk 04/04/2025
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.