Nipro Blood Tubing set with Priming Set and Transducer Protectors — Class II medical device recall Z-1876-2018
Terminated recall by Nipro Medical Corporation, reported 2018-05-23, distributed in GA, NY, TN, TX. There is a possibility of the heparin line is occluded.
| Recall number | Z-1876-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nipro Medical Corporation, Doral, FL, United States |
| Recall initiated | 2017-12-19 |
| Classified | 2018-05-15 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2021-10-19 |
| Distributed | GA, NY, TN, TX |
| Quantity | 307,944 units |
| Lot numbers | 17I01-9, 17I06-9, 17I16-9, 17I18-9, 17I19-9, 17I21-9, 17I25-9, 17I26-9, 17J09-9, 17J11-9, 17J12-9, 17J16-9, 17J17-9, 17J19-9, 17J20-9, 17J21-9, 17K07-9, 17K15-9, 17K16-9 |
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.
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-1876-2018. 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.