Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026

Presource Convenience Kits

Cardinal Health 200, LLC

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

Is this the product you have?

Presource Convenience Kits

19 of 19 products

Products covered by this recall
Model / numberProduct as published
AMN548616AKIT, PRE OP
BA1DH0116BKIT, NICU ADMIT NEW HAN
IVSJV8302EKIT, PRE PROCEDURE
IVS3223531KIT, IV SUPPLIES
IVS3223532KIT, IV SUPPLIES
IVS3223533KIT, IV SUPPLIES
IVS3223534KIT, IV SUPPLIES
IVS3223535KIT, IV SUPPLIES
IVS322358MKIT, IV SUPPLIES
IVS322358NKIT, IV SUPPLIES
IVS322358OKIT, IV SUPPLIES
AMN333032AKIT, PATIENT ADMISSIONS
MAT42267ALKIT, C SECTION
MAT4226725KIT, C SECTION
MAT422677GKIT, VAGINAL DELIVERY
MAT4226792KIT, VAGINAL DELIVERY
MAT4226793KIT, VAGINAL DELIVERY
MAT4226794KIT, VAGINAL DELIVERY
MAT4226795KIT, VAGINAL DELIVERY
Lot codes and dates

91 of 91 products

Products covered by this recall
#BarcodesProduct as published
11019895600633110198956006331Lot Number: 4249818 ; 2) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
21019895600633110198956006331Lot Number: 5124984 ; 3) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
31019895600633110198956006331Lot Number: 5129488 ; 4) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
41019895600633110198956006331Lot Number: 5129488 ; 5) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
51019895600633110198956006331Lot Number: 5188103 ; 6) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
61019895600633110198956006331Lot Number: 5188103 ; 7) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
71019895600633110198956006331Lot Number: 5211212 ; 8) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
81019895600633110198956006331Lot Number: 5155824 ; 9) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
91019895600633110198956006331Lot Number: 5211985 ; 10) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
101019895600633110198956006331Lot Number: 5279226 ; 11) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
111019895600633110198956006331Lot Number: 5155824 ; 12) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
121019895600633110198956006331Lot Number: 5188103 ; 13) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
131019895600633110198956006331Lot Number: 5211212 ; 14) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
141019895600633110198956006331Lot Number: 5246952 ; 15) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
151019895600633110198956006331Lot Number: 5279226 ; 16) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
161019895600633110198956006331Lot Number: 5279226 ; 17) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
171019895600633110198956006331Lot Number: 6062168 ; 18) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
181019895600633110198956006331Lot Number: 5155824 ; 19) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
191019895600633110198956006331Lot Number: 5279226 ; 20) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case)
20Lot Number: 6062168 ; 21) BA1DH0116B, UDI-DI: 0(each), 0(case)
Amount recalled
17503 kits

This recall covers 2 products

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

Where it was sold

Why it was recalled

The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient harm or may lead to localized skin or soft tissue infection. Less commonly, systemic infection or other infectious complications may occur.

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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 12:27 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.