PlainRecalls
FDA Devices Moderate Class II Ongoing

Proteus235- Proton Therapy System: to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation

Reported: June 8, 2022 Initiated: April 20, 2022 #Z-1205-2022

Product Description

Proteus235- Proton Therapy System: to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation

Reason for Recall

First layer of Uniform Scanning treatment fields is sometimes irradiated with incorrect Scanning Magnet setpoints resulting in the field size may be smaller than expected and the irradiated area may receive more dose than prescribed

Details

Units Affected
4 units
Distribution
Worldwide distribution - US Nationwide distribution in the states of IL, VA, WA and the country of Germany.
Location
Louvain-la-neuve, N/A

Frequently Asked Questions

What product was recalled?
Proteus235- Proton Therapy System: to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. Recalled by Ion Beam Applications S.A.. Units affected: 4 units.
Why was this product recalled?
First layer of Uniform Scanning treatment fields is sometimes irradiated with incorrect Scanning Magnet setpoints resulting in the field size may be smaller than expected and the irradiated area may receive more dose than prescribed
Which agency issued this recall?
This recall was issued by the FDA Devices on June 8, 2022. Severity: Moderate. Recall number: Z-1205-2022.