Fresenius Liberty Cycler Set Single Conn — Class II medical device recall Z-1674-2013
Terminated recall by Fresenius Medical Care Holdings, Inc., reported 2013-07-17, distributed nationwide. Cassette may leak during set up or during peritoneal dialysis treatment
| Recall number | Z-1674-2013 |
|---|---|
| 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 | 2013-06-03 |
| Classified | 2013-07-10 |
| Reported by FDA | 2013-07-17 |
| Terminated | 2014-06-18 |
| Distributed | Nationwide (US) |
| Quantity | 5,480 units |
| Reason classes | packaging |
| Lot numbers | 11PR08083 |
Product
Fresenius Liberty Cycler Set Single Conn./Ext DL Product Number: 050-87216 Automated Peritoneal Dialysis System with integrated stay safe patient connector and extended drain line.
Reason for recall
Cassette may leak during set up or during peritoneal dialysis treatment
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-1674-2013. 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.