Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Segmented Cervix Applicator Set Recalled by Varian Medical Systems, Inc. Due to The guide tube which is part of the...
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 Cervix Applicator Set, part number GM11004310, a component used with the tube for segments and cervical sleeves The guide tube for segments and cervical sleeves in the Segmented Cervix Applicator Set was developed to treat cancer of the cervix, vagina, endometrium, vaginal stump and uterus. It is used for Brachytherapy.
Quantity: 15 units
Why Was This Recalled?
The guide tube which is part of the Segmented Cervix Applicator Set is difficult to disconnect from cervical sleeve.
Where Was This Sold?
Worldwide Distribution - U.S. state of Georgia and the countries of Canada, Germany, India, Poland, and Thailand.
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