Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: Catalyst+ Product Name: C4D software used in conjunction Recalled by C-RAD POSITIONING AB Due to Software issue with scanning equipment that can results...
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 C-RAD POSITIONING AB directly.
Affected Products
Brand Name: Catalyst+ Product Name: C4D software used in conjunction with Catalyst (SP001-0025), Catalyst HD (SP001-0026), Catalyst PT (SP001-0027), Catalyst X4 (SP002-0035), Catalyst+ (SP003-0001), Catalyst+ HD (SP003-0002), Catalyst+ PT (SP003-0008), Catalyst+ X4, (SPOO3-0009) Product Description: Patient positioning device, diagnostic imaging/radiotherapy, laser Component: Not a component
Quantity: 44 units
Why Was This Recalled?
Software issue with scanning equipment that can results in the filed rotation not being applied correctly.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About C-RAD POSITIONING AB
C-RAD POSITIONING AB has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report