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?

67 of 67 products

Products covered by this recall
Model / numberProduct as published
MA1DH7533CKIT, ANTEPARTUM IV
MAT4226716KIT, C SECTION
MAT4226780KIT, VAGINAL DELIVERY
OVCVM01028KIT, CVR
MAT4226715KIT, C SECTION
OVCVM01027KIT, CVR
MAT4226714KIT, VAGINAL DELIVERY
OROMH47346KIT, LABOR ADMISSION
OVCVM01026KIT, CVR
MAT4226779KIT, VAGINAL DELIVERY
MAT4226713KIT, C SECTION
MAT422677DKIT, VAGINAL DELIVERY
MAT4226778KIT, VAGINAL DELIVERY
OVCVM01025KIT, CVR
MAT4226712KIT, C SECTION
OVCVM01024KIT, CVR
OVCVM01023KIT, CVR
OVCVM01022KIT, CVR
OROMH47345KIT, LABOR ADMISSION
OVCVM01021KIT, CVR
Lot codes and dates

1,561 of 1,561 products

Products covered by this recall
Model / numberBarcodesProduct as published
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 584713
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 584713
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 584713
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 584713
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 585725
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 585725
1088843999705750888439997055CATALOG #MA1DH7533C, (ea) 50888439997055 (cs), LOT # 585725
1088843998977950888439989777CATALOG #MAT4226716, (ea) 50888439989777 (cs), LOT # 554018
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998611250888439986110CATALOG #MAT4226780, (ea) 50888439986110 (cs), LOT # 551641
1088843998600650888439986004CATALOG #OVCVM01028, (ea) 50888439986004 (cs), LOT # 551639
1088843998600650888439986004CATALOG #OVCVM01028, (ea) 50888439986004 (cs), LOT # 551639
1088843998600650888439986004CATALOG #OVCVM01028, (ea) 50888439986004 (cs), LOT # 551639
1088843998600650888439986004CATALOG #OVCVM01028, (ea) 50888439986004 (cs), LOT # 551639
1088843998600650888439986004CATALOG #OVCVM01028, (ea) 50888439986004 (cs), LOT # 551639
Amount recalled
415636 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.