Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and… — Class II medical device recall Z-0693-2016
Terminated recall by Fresenius Medical Care Renal Therapies Group, LLC, reported 2016-02-03, distributed nationwide. The door latch may not fully close and the door may open unexpectedly. The door may make physical contact with
| Recall number | Z-0693-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fresenius Medical Care Renal Therapies Group, LLC, Waltham, MA, United States |
| Recall initiated | 2015-12-15 |
| Classified | 2016-01-27 |
| Reported by FDA | 2016-02-03 |
| Terminated | 2019-10-07 |
| Distributed | Nationwide (US) |
| Quantity | 14,094 units |
| Model numbers | 180111, RTLR180111 |
Product
Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and RTLR180111
Reason for recall
The door latch may not fully close and the door may open unexpectedly. The door may make physical contact with anything near the door of the machine, including the patient. May cause injury, delay in treatment, or Increased Intraperitoneal Volume (IIPV) (overfill).
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-0693-2016. 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.