Urgent Field Safety Notice For Arvis Hip And Knee Tracking And Positioning Instrumentation By Kico Knee Innovation Company Pty Ltd
Recall Summary ARVIS Hip and Knee Tracking and Positioning Instrumentation devices made by Kico Knee Innovation Company Pty Ltd are being recalled in Germany and the EU. The devices are classified as a Class I recall, the most serious type. The specific safety concern and details about which models or serial numbers are affected are not clearly stated in the available information.
- Recalling firm
- Urgent Field Safety Notice for ARVIS Hip and Knee Tracking and Positioning Instrumentation by Kico Knee Innovation Compa
- Product
- s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for ARVIS Hip and Knee Tracking and Positioning Instrumentation by Kico Knee Innovation Company Pty Ltd 2026
- Reason
- assessment Field corrective actions Urgent Field Safety Notice for ARVIS Hip and Knee Tracking and Positioning Instrumentation by Kico Knee Innovation Company Pty Ltd 2026
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-06-09
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/621d968e-281f-45dd-9b44-628aacc8ae53