Fresenius Liberty Cycler Set Single Conn — Class II medical device recall Z-0799-2013
Terminated recall by Fresenius Medical Care Holdings, Inc., reported 2013-02-20, distributed nationwide. There is a small risk of a leak in Cycler Sets and if the Cycler Set is punctured, the dialysate may become co
| Recall number | Z-0799-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fresenius Medical Care Holdings, Inc., Waltham, MA, United States |
| Recall initiated | 2012-10-12 |
| Classified | 2013-02-11 |
| Reported by FDA | 2013-02-20 |
| Terminated | 2020-12-30 |
| Distributed | Nationwide (US) |
| Reason classes | packaging |
| Lot numbers | 12BR08009 |
| Model numbers | 050-87216 |
Product
Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: 050-87216. Acute and chronic peritoneal dialysis.
Reason for recall
There is a small risk of a leak in Cycler Sets and if the Cycler Set is punctured, the dialysate may become contaminated potentially resulting in peritonitis.
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-0799-2013. 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.