FDA Device recall Z-0760-2013
Rectal Retractors, titanium, item # AL07368000, a component of Varian Medical Ring and Tandem Applicator Sets
- FDA Device
- Class II
- terminated
- Published 2013-02-06
On 2013-02-06 the FDA classified a Class II recall of Rectal Retractors, titanium, item # AL07368000, a component of Varian Medical Ring and Tandem Applicator Sets by Varian Medical Systems, citing A medical device used in brachytherapy may become contaminated and can cause infections, toxicity or allergic reactions.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0760-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-12 |
| Published | 2013-02-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Varian Medical Systems |
| Distribution | US |
Product
Rectal Retractors, titanium, item # AL07368000, a component of Varian Medical Ring and Tandem Applicator Sets; Intended for use in Brachytherapy.
Reason
A medical device used in brachytherapy may become contaminated and can cause infections, toxicity or allergic reactions.
Identifiers
| code_info | All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0760-2013%22
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