Rectal Retractors — Class II medical device recall Z-0760-2013
Terminated recall by Varian Medical Systems, Inc., reported 2013-02-06, distributed nationwide. A medical device used in brachytherapy may become contaminated and can cause infections, toxicity or allergic
| Recall number | Z-0760-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Varian Medical Systems, Inc., Charlottesville, VA, United States |
| Recall initiated | 2012-04-12 |
| Classified | 2013-01-31 |
| Reported by FDA | 2013-02-06 |
| Terminated | 2014-04-10 |
| Distributed | Nationwide (US) |
| Quantity | 152 units |
| Model numbers | AL07368000 |
Product
Rectal Retractors, titanium, item # AL07368000, a component of Varian Medical Ring and Tandem Applicator Sets; Intended for use in Brachytherapy.
Reason for recall
A medical device used in brachytherapy may become contaminated and can cause infections, toxicity or allergic reactions.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0760-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.