Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Segmented Cylinder Applicator Set Recalled by Varian Medical Systems, Inc. Due to Segmented cylinder applicator set may slip during treatment,...
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 Varian Medical Systems, Inc. directly.
Affected Products
Segmented Cylinder Applicator Set, Model # GM11004150, when used for Pulsed Dose Rate (PDR) Product Usage: Usage: Used during pulsed dose rate brachytherapy to treat vaginal and rectal cancer.
Quantity: 21 devices
Why Was This Recalled?
Segmented cylinder applicator set may slip during treatment, causing the delivery of radiation to areas outside the target.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Varian Medical Systems, Inc.
Varian Medical Systems, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report