Proteus235- Proton Therapy System: to produce and deliver a proton beam for the treatment of patients with localized tu
Summary
The FDA issued a Class II for Proteus235- Proton Therapy System: to produce and deliver a proton beam for the by Ion Beam Applications S.A.. Reason: First layer of Uniform Scanning treatment fields is sometimes irradiated with incorrect Scanning Magnet setpoints resulting in the field size may be s.
Details
Source
Device Recall
External ID
Z-1205-2022
Action Date
2022-06-08
Status
Ongoing
Category
device
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
Lot/Code Info: UDI-DI: (01)05404013801138 Serial Numbers: PAT108 (US), PAT112 (US), SAT116 (US). PAT107 (EU).
Quantity Affected: 4 units
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
Distribution
Worldwide distribution - US Nationwide distribution in the states of IL, VA, WA and the country of Germany.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-20
Company
Louvain-la-neuve, N/A
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 184 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Ion Beam Applications S.A. has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ion Beam Applications S.A.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ion Beam Applications S.A. have FDA actions?
Ion Beam Applications S.A. has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1205-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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