Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Proteus ONE and Proteus Plus Recalled by Ion Beam Applications S.A. Due to IBA is initiating this recall to notify its...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ion Beam Applications S.A. directly.
Affected Products
Proteus ONE and Proteus Plus
Quantity: N/A
Why Was This Recalled?
IBA is initiating this recall to notify its customers that the use of non-IBA accessories and/or third party equipment or unauthorized modifications to an IBA medical device may pose a safety risk.
Where Was This Sold?
Units were delivered in the USA, Korea, Germany, France, Czech Republic, Italy, Poland and Sweden.
About Ion Beam Applications S.A.
Ion Beam Applications S.A. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report