# FDA recall Z-2151-2019

> **Fresenius Medical Care Renal Therapies Group, LLC** · Class II · device recall initiated 2019-05-29.

## 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.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2151-2019
- **Recalling firm:** Fresenius Medical Care Renal Therapies Group, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-29
- **Report date:** 2019-08-14
- **Termination date:** 2020-11-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waltham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2151-2019

## Citation

> AI Analytics. FDA recall Z-2151-2019. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2151-2019. Source: US FDA. Licensed CC0.

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