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
| Model / number | Product as published |
|---|---|
AMN548616A | KIT, PRE OP |
BA1DH0116B | KIT, NICU ADMIT NEW HAN |
IVSJV8302E | KIT, PRE PROCEDURE |
IVS3223531 | KIT, IV SUPPLIES |
IVS3223532 | KIT, IV SUPPLIES |
IVS3223533 | KIT, IV SUPPLIES |
IVS3223534 | KIT, IV SUPPLIES |
IVS3223535 | KIT, IV SUPPLIES |
IVS322358M | KIT, IV SUPPLIES |
IVS322358N | KIT, IV SUPPLIES |
IVS322358O | KIT, IV SUPPLIES |
AMN333032A | KIT, PATIENT ADMISSIONS |
MAT42267AL | KIT, C SECTION |
MAT4226725 | KIT, C SECTION |
MAT422677G | KIT, VAGINAL DELIVERY |
MAT4226792 | KIT, VAGINAL DELIVERY |
MAT4226793 | KIT, VAGINAL DELIVERY |
MAT4226794 | KIT, VAGINAL DELIVERY |
MAT4226795 | KIT, VAGINAL DELIVERY |
- Lot codes and dates
91 of 91 products
Products covered by this recall # Barcodes Product as published 1 1019895600633110198956006331Lot Number: 4249818 ; 2) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 2 1019895600633110198956006331Lot Number: 5124984 ; 3) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 3 1019895600633110198956006331Lot Number: 5129488 ; 4) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 4 1019895600633110198956006331Lot Number: 5129488 ; 5) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 5 1019895600633110198956006331Lot Number: 5188103 ; 6) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 6 1019895600633110198956006331Lot Number: 5188103 ; 7) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 7 1019895600633110198956006331Lot Number: 5211212 ; 8) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 8 1019895600633110198956006331Lot Number: 5155824 ; 9) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 9 1019895600633110198956006331Lot Number: 5211985 ; 10) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 10 1019895600633110198956006331Lot Number: 5279226 ; 11) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 11 1019895600633110198956006331Lot Number: 5155824 ; 12) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 12 1019895600633110198956006331Lot Number: 5188103 ; 13) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 13 1019895600633110198956006331Lot Number: 5211212 ; 14) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 14 1019895600633110198956006331Lot Number: 5246952 ; 15) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 15 1019895600633110198956006331Lot Number: 5279226 ; 16) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 16 1019895600633110198956006331Lot Number: 5279226 ; 17) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 17 1019895600633110198956006331Lot Number: 6062168 ; 18) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 18 1019895600633110198956006331Lot Number: 5155824 ; 19) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 19 1019895600633110198956006331Lot Number: 5279226 ; 20) BA1DH0116B, UDI-DI: 10198956006331(each), 10198956006331(case) 20 Lot 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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