Data Foundry

Medical device recalls 2019

Liberty Cycler Cassettes — Class II medical device recall Z-2151-2019

Terminated recall by Fresenius Medical Care Renal Therapies Group, LLC, reported 2019-08-14, distributed nationwide. Additional Instructions: step-by step handling and inserting the cassette into the Liberty Cycler set. A damag

Recall numberZ-2151-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmFresenius Medical Care Renal Therapies Group, LLC, Waltham, MA, United States
Recall initiated2019-05-29
Classified2019-08-05
Reported by FDA2019-08-14
Terminated2020-11-19
DistributedNationwide (US)
Reason classespackaging
Model numbers050-87212, 050-87215, 050-87216

Product

Liberty Cycler Cassettes (a disposable cassette that is intended to be used to perform peritoneal dialysis (APD) in conjunction with the Liberty cycler as follows: (1) LIBERTY Line Cycler Set with Stay-safe connectors (Dual Patient Connector) Part Number: 050-87212 (2) LIBERTY Line Cycler Set with Stay-safe connectors (Single Patient Connector) Part Number: 050-87215 (3) LIBERTY Integrated Cycler Set with single Stay-safe patient connector and extended drain line Part Number: 050-87216

Reason for recall

Additional Instructions: step-by step handling and inserting the cassette into the Liberty Cycler set. A damaged cassette can cause peritoneal dialysis (PD) solution to leak into the cycler and is a potential risk for contamination.

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-2151-2019. 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.