FDAClass IIJanuary 20, 2016

NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis recall

NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable bloodline intended to provide…

Why was NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis recalled?

Blood foaming was found during evaluation of the product.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #'s 13E02, 13E03, 13E06, 13E07, 13E08,13E09, 13E10, 13G03, 13G11, 13G15, 14G24, 13G30, and 13H06.

Product
NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable bloodline intended to provide…
Recalling firm
Nipro Medical Corporation
Quantity
1,484 pieces.
Distribution
US Distribution to states of: TN and NJ.
Recall date
January 20, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls