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Varian Medical Systems, Inc. recalls Segmented Cervix Applicator Set, part number GM11004310, a component used with the tube for segments and cervical sleeve
Recalled December 26, 2012 · FDA recall Z-0607-2013 · Varian Medical Systems
Hazard
The guide tube which is part of the Segmented Cervix Applicator Set is difficult to disconnect from cervical sleeve. · FDA Class II
Units
15 units
Sold at
Worldwide Distribution - U.S. state of Georgia and the countries of Canada, Germany, India, Poland, and Thailand.
Description
The guide tube which is part of the Segmented Cervix Applicator Set is difficult to disconnect from cervical sleeve.
Product
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.
Manufacturer(s)
Varian Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →