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
100020070810002031171000203118100020311910002031201000203121100020567810002058971000205898100020589910002059001000205901100020687210002068731000206874100020824710002082481000208249100020825010002103141000210315100021031610002103171000210318100021031910002103201000211719100021172010002117211000211722100021172310002117241000215485100021548610002154871000215488100021548910002154901000217361100021736210002173631000217364100021886610002188671000218868100021886910002188701000218871100022052910002205301000220531100022053210002230701000223071100022307210002230731000223074100022542710002254281000225429
- 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.
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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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