Ion Beam Applications recalls

Ion Beam Applications has 36 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 18 Mar 2026. 10 are still ongoing. 1 was reported in the last 12 months.

Total recalls36since 2014
Last 12 months1reported
Class I00% of total
Ongoing10latest 18 Mar 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 36 100%Class III 0 0%

Why ion beam applications is recalled

By year

Ongoing ion beam applications recalls

10 active

All ion beam applications recalls, newest first

36 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIIBA Proton Therapy System - Proteus recalled by Ion Beam ApplicationsIon Beam ApplicationsDevice MalfunctionNationwide
DeviceCLASS IIIBA Proton Therapy System - Proteus 235 ProteusPLUS and ProteusONE recalledIon Beam ApplicationsDevice MalfunctionNationwide
DeviceCLASS IIIBA Proton Therapy System - Proteus 235- Designed recalledIon Beam ApplicationsOther9 states
DeviceCLASS IIIBA Proton Therapy System - Proteus recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherNationwide
DeviceCLASS IIIba Proton Therapy System - Proteus 235, Pts-10 versions recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIIBA Proton Therapy System - Proteus recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteus235- Proton Therapy System: to produce recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteusPLUS and ProteusONE- designed to produce recalledIon Beam ApplicationsDevice Malfunction12 states
DeviceCLASS IIProteus 235; Version: Pts-8 versions before Pts recalledIon Beam ApplicationsDevice Malfunction4 states
DeviceCLASS IIProteus 235- designed to produce recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteus 235-Proton Therapy System recalled by Ion Beam ApplicationsIon Beam ApplicationsOther5 states
DeviceCLASS IIProteus 235 The Proton Therapy System - Proteus recalledIon Beam ApplicationsDevice MalfunctionNationwide
DeviceCLASS IIProteus 235 The Proton Therapy System - Proteus recalledIon Beam ApplicationsOtherVA
DeviceCLASS IIProteus 235 Product Usage: The Proton Therapy System - Proteus recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteus 235, Universal Nozzle with snout recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteus 235, Version Pts-11.0.1.2 and Pts-11.0.2 Product Usage recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIThe Proton Therapy System - Proteus 235 (brand names recalledIon Beam ApplicationsDevice MalfunctionFL
DeviceCLASS IIProteus 235 The PTS is a medical device designed to produce recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIRecalled product recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherN/A
DeviceCLASS IIProteus ONE and Proteus Plus recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherN/A
DeviceCLASS II12C (AdaPTinsight) component: AdaPTinsight recalledIon Beam ApplicationsDevice MalfunctionNationwide
DeviceCLASS IIProteus 235, ProteusPLUS or Proteus ONE produces recalledIon Beam ApplicationsOther4 states
DeviceCLASS IIProteus 235, Uniform and Pencil Beam Scanning The Proton recalledIon Beam ApplicationsOther6 states
DeviceCLASS IIProteus 235, Proton Therapy System a medical device recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteus 235, Pencil Beam Scanning, Pts-9.4.X recalledIon Beam ApplicationsOtherNationwide
DeviceCLASS IIProteus 235, graphite block recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherWA
DeviceCLASS IIProteus 235, Pencil Beam Scanning recalled by Ion Beam ApplicationsIon Beam ApplicationsOtherFL
DeviceCLASS IIProteus 235 and Proteus ONE proton therapy systems recalledIon Beam ApplicationsDevice Malfunction10 states
DeviceCLASS IIProteus 235, Proton Therapy System recalled by Ion Beam ApplicationsIon Beam ApplicationsDevice Malfunction5 states
DeviceCLASS IIProteus recalled by Ion Beam ApplicationsIon Beam ApplicationsOther10 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.