Nipro recalls blood tubing sets with possible heparin line occlusion. Affected units include specific model numbers and batch dates. Contact Nipro for details.
There is a possibility of the heparin line is occluded.
Nipro is recalling blood tubing sets used in hemodialysis that may cause heparin lines to become blocked. This could lead to complications during dialysis treatment if not addressed.
The heparin line in the tubing set could become blocked, potentially causing issues with blood flow during hemodialysis. This might require additional treatment or intervention.
Healthcare professionals using hemodialysis equipment are most at risk. Patients undergoing dialysis may be affected if the tubing set is used.
Check for model numbers BL+A223D/V809D and batch numbers listed in the recall notice. The product comes in film pouches with 24 lines per case.
Identify the model number and batch number on the film pouch packaging.
The model number is BL+A223D/V809D.
Affected batch numbers include 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.
Look for the model number BL+A223D/V809D and the specific batch numbers listed in the recall notice.
We’ve drafted a message you can send Nipro to request your refund or repair — edit it as you like.
Subject: Recall Z-1876-2018 — Nipro Nipro Hello, I own a Nipro that is covered by recall Z-1876-2018 from Nipro. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.