Usingen, Germany
Klinika Mdical Gmb recalls
1 recall recorded since 2018, most recently on 4 April 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 4 April 2025
- Reason
- Potential for microbial contamination.
- Distribution
- US Nationwide distribution in the state of Massachusetts.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1769-2025, Z-1768-2025
- 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 o
- KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during su
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.