In the agency's Nov 11, 2026 enforcement report · Ongoing

Cardinal Health Presource PBDS kits, Containing BD Alaris Pump Infusion Sets used with BD Alaris Pump Module Model…

Cardinal Health 200, LLC

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337

Is this the product you have?

33 of 33 products

Products covered by this recall
Model / numberProduct as published
IVS5342277IV START LD KIT
IVS5342276IV START LD KIT
IVS5342275IV START LD KIT
IVS5342274IV START LD KIT
IVS5342273IV START LD KIT
IVS5342272IV START LD KIT
IVS5342271IV START LD KIT
IVS534227BIV START LD KIT
BLDV125142IV START BLOOD DRAW,KIT
SPKVM01011RUN W/O SPKVM0102X
BLDHD03262IV START BLOOD DRAW, KIT
BLDHD0326CIV START BLOOD DRAW, KIT
BLDV125141IV START BLOOD DRAW,KIT
BLDHD03261IV START BLOOD DRAW,KIT
BLDV12514AKIT,IV START BLOOD DRAW
IVSJV83001KIT,IV START
IVS534227AIV START LD KIT
—IV START BLOOD DRAW,KIT , CATALOG # PLHDBDHCH
—IV START BLOOD DRAW, KIT , CATALOG # PLHDBDHCG
—IV START, ,KIT , CATALOG # PJJVIVMMU
Lot codes and dates

539 of 539 products

Products covered by this recall
Model / numberBarcodesProduct as published
1088843996781450888439967812CATALOG # IVS5342277, (ea) 50888439967812 (cs), LOT #540480
1088843996781450888439967812CATALOG # IVS5342277, (ea) 50888439967812 (cs), LOT #540480
1088843982069050888439820698CATALOG # IVS5342276, (ea) 50888439820698 (cs), LOT #425675
1088843982069050888439820698CATALOG # IVS5342276, (ea) 50888439820698 (cs), LOT #425675
1088843979362850888439793626CATALOG # IVS5342275, (ea) 50888439793626 (cs), LOT #404845
1088843979362850888439793626CATALOG # IVS5342275, (ea) 50888439793626 (cs), LOT #404845
1088843979362850888439793626CATALOG # IVS5342275, (ea) 50888439793626 (cs), LOT #404845
1088843979362850888439793626CATALOG # IVS5342275, (ea) 50888439793626 (cs), LOT #404845
1088843978381050888439783818CATALOG # IVS5342274, (ea) 50888439783818 (cs), LOT #395356
1088843978381050888439783818CATALOG # IVS5342274, (ea) 50888439783818 (cs), LOT #395356
1088843967618150888439676189CATALOG # IVS5342273, (ea) 50888439676189 (cs), LOT #365114
1088843967618150888439676189CATALOG # IVS5342273, (ea) 50888439676189 (cs), LOT #365114
1088843962646950888439626467CATALOG # IVS5342272, (ea) 50888439626467 (cs), LOT #331290
1088843962646950888439626467CATALOG # IVS5342272, (ea) 50888439626467 (cs), LOT #331290
1088843954291250888439542910CATALOG # IVS5342271, (ea) 50888439542910 (cs), LOT #267592
1088843954291250888439542910CATALOG # IVS5342271, (ea) 50888439542910 (cs), LOT #267592
1088843954291250888439542910CATALOG # IVS5342271, (ea) 50888439542910 (cs), LOT #267592
1088843941921450888439419212CATALOG # IVS534227B, (ea) 50888439419212 (cs), LOT #208006
1088843941921450888439419212CATALOG # IVS534227B, (ea) 50888439419212 (cs), LOT #208006
1088843941921450888439419212CATALOG # IVS534227B, (ea) 50888439419212 (cs), LOT #208006
Amount recalled
221554 kits

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Why it was recalled

Stop using this product now

Kits contain infusion sets which were recalled for performance issues.

Using this product could cause serious injury, illness or death — stop using it now.

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 (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Nov 4, 12:28 AM 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.