Mevion Medical Systems, Inc. recalls MEVION S250 Radiation therapy system
- Recall date
- November 18, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0767-2016
- FDA classification
- Class II
- Brand / firm
- Mevion Medical Systems, Inc.
- Sold / distributed
- US nationwide distribution including FL, NJ, OK, and MO.
Why it was recalled
The treatment table positioning belt can slip gear positions, resulting in deviation of patient setup and treatment positions from the time of slippage until the discovery of slippage and the halting of treatment.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
MEVION S250 Radiation therapy system
Get recall alerts
Free email alert whenever Mevion Medical Systems, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Mevion Medical Systems, Inc.