# FDA recall Z-1876-2018

> **Nipro Medical Corporation** · Class II · device recall initiated 2017-12-19.

## Product

Nipro Blood Tubing set with Priming Set and Transducer Protectors.  Each device is packaged in a film pouch with 24 lines per case.      The Nipro¿ Set - Blood Tubing Set with Transducer Protector and Priming Set are disposable bloodlines intended to provide extracorporeal access to the patient s blood during hemodialysis. The compatibility of available configurations is the responsibility of the physician in charge.

## Reason for recall

There is a possibility of the heparin line is occluded.

## Distribution

US Distribution to the states of :  GA, NY, TN, TX.

## Key facts

- **Recall number:** Z-1876-2018
- **Recalling firm:** Nipro Medical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-19
- **Report date:** 2018-05-23
- **Termination date:** 2021-10-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Doral, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1876-2018

## Citation

> AI Analytics. FDA recall Z-1876-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1876-2018. Source: US FDA. Licensed CC0.

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