Proteus 235, Proton Therapy System
Reported: April 26, 2017 Initiated: March 21, 2017 #Z-1830-2017
Product Description
Proteus 235, Proton Therapy System
Reason for Recall
In specific circumstances, the user is able to restart an aborted irradiation without having to select the correct partial irradiation data.
Details
- Recalling Firm
- Ion Beam Applications S.A.
- Units Affected
- 2 worldwide, 1 in U.S.
- Distribution
- Distribution in US (to Louisiana), and France.
- Location
- Louvain La Neuve, N/A
Frequently Asked Questions
What product was recalled? ▼
Proteus 235, Proton Therapy System. Recalled by Ion Beam Applications S.A.. Units affected: 2 worldwide, 1 in U.S..
Why was this product recalled? ▼
In specific circumstances, the user is able to restart an aborted irradiation without having to select the correct partial irradiation data.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 26, 2017. Severity: Moderate. Recall number: Z-1830-2017.
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