Urgent Field Safety Notice For Cervical/intrauterine Brachytherapy System By Elekta Nucletron B.v
Elekta Nucletron B.V. has issued an urgent safety notice for its cervical/intrauterine brachytherapy systems used in cancer treatment. The notice is classified as Class I, indicating a serious issue, and affects devices distributed in Germany and the EU. The specific reason for the safety notice is not detailed in this summary.
- Recalling firm
- Elekta Nucletron B.V
- Product
- Cervical/intrauterine brachytherapy system
- Reason
- Urgent Field Safety Notice for Cervical/intrauterine brachytherapy system by Elekta Nucletron B.V
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-06-02
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/9ff9e7cc-43e3-4dd9-a430-f77d16895298