Reflexion Medical, Inc.: Fludeoxyglucose F18-guided Radiation Therapy System
- Recalling firm
- Reflexion Medical, Inc.
- Product
- RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00
- Reason
- Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the initial localization scan are not carried through to treatment delivery leading to the treatment plan dose being delivered to the incorrect location, potentially a displacement of 5mm or higher, with a 10% to 20% underdose.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-02-09
- Status
- Open, Classified
- Areas affected
- CA, CT, LA, NJ, OH, OR, PA, TX
- Distribution
- US: CA, TX, PA, CT, NJ, OR, LA, OH
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5805fb70-4797-4848-8fcb-a3b71dae12f1