Reported Jun 10, 2020 · Terminated

Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis treatment using…

Baxter Healthcare 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: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Gambro Cartridge
  • Blood Set Prime Line - Product Usageis intended for single use in a hemodialysis treatment using Dialysis Delivery Systems
Lot codes and dates
  • Product Code101025
  • UDI37332414007837
  • Lot Numbers

    65 of 65 codes

    • 1000200708
    • 1000203117
    • 1000203118
    • 1000203119
    • 1000203120
    • 1000203121
    • 1000205678
    • 1000205897
    • 1000205898
    • 1000205899
    • 1000205900
    • 1000205901
    • 1000206872
    • 1000206873
    • 1000206874
    • 1000208247
    • 1000208248
    • 1000208249
    • 1000208250
    • 1000210314
    • 1000210315
    • 1000210316
    • 1000210317
    • 1000210318
    • 1000210319
    • 1000210320
    • 1000211719
    • 1000211720
    • 1000211721
    • 1000211722
    • 1000211723
    • 1000211724
    • 1000215485
    • 1000215486
    • 1000215487
    • 1000215488
    • 1000215489
    • 1000215490
    • 1000217361
    • 1000217362
    • 1000217363
    • 1000217364
    • 1000218866
    • 1000218867
    • 1000218868
    • 1000218869
    • 1000218870
    • 1000218871
    • 1000220529
    • 1000220530
    • 1000220531
    • 1000220532
    • 1000223070
    • 1000223071
    • 1000223072
    • 1000223073
    • 1000223074
    • 1000225427
    • 1000225428
    • 1000225429
Amount recalled
2,361,885 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

Potential disconnection of tubing set.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 7, 2023 · Data as of Sep 19, 5:26 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.