Reported May 23, 2018 · Terminated

Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24…

Nipro Medical Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Nipro Medical Corporation · 3150 NW 107th Ave · Doral, FL · 33172-2135

Is this the product you have?

  • 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.
Lot codes and dates
    • Model No. BL+A223D/V809D
    • Vendor Batch No. 17I06-9
    • 17I16-9
    • 17I18-9
    • 17J17-9
    • 17J19-9
    • 17J20-9
    • 17J21-9
    • 17I19-9
    • 17K07-9
    • 17I01-9
    • 17J12-9
    • 17J16-9
    • 17I21-9
    • 17I25-9
    • 17I26-9
    • 17J09-9
    • 17J11-9
    • 17K15-9
    • 17K16-9
Amount recalled
307,944 units.

Where it was sold

Why it was recalled

There is a possibility of the heparin line is occluded.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 19, 2021 · Data as of Sep 19, 6:06 PM UTC

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