Reported Aug 19, 2026 · Ongoing · Updated Aug 25, 2026
Cardinal Health Presource 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?
Cardinal Health Presource Kits
10 of 10 products
| Model / number | Product as published |
|---|---|
SEN73NSKCF | SEPTO RHINO PACK |
SNE30CNOHE | PACK NEURO MINOR CRANIOTOMY |
SNE30CRJGY | NEURO MAJOR 2 PACK |
SNE43NEE13 | NEURO PACK |
SNE43NEE13 | LAMINECTOMY PACK |
SNE5CLPB13 | LAMINECTOMY PACK |
SNE69PSKR4 | PEDI SPINE R |
SNE7CSHY15 | SHUNT PACK |
SNE7CSHY16 | SHUNT PACK |
SOP30ODSCL | ENS ORTHO FUSION POSTERIEURE 3 |
- Lot codes and dates
11 of 11 products
Products covered by this recall # Barcodes Product as published 1 1019559450623050195594506238Lot Number: 3024-2 ; 2) SNE30CNOHE, UDI-DI: 10195594506230(each), 50195594506238(case) 2 1019559445399250195594453990Lot Number: 93845 ; 3) SNE30CRJGY, UDI-DI: 10195594453992(each), 50195594453990(case) 3 1019895647096550198956470963Lot Number: 4730 ; 4) SNE43NEE13, UDI-DI: 10198956470965(each), 50198956470963(case) 4 1019710626668750197106266685Lot Number: 14039 ; 5) SNE5CLPB12, UDI-DI: 10197106266687(each), 50197106266685(case) 5 1019710626668750197106266685Lot Number: 6033 ; 6) SNE5CLPB12, UDI-DI: 10197106266687(each), 50197106266685(case) 6 1019710632813250197106328130Lot Number: 4366 ; 7) SNE5CLPB13, UDI-DI: 10197106328132(each), 50197106328130(case) 7 1019710689558050197106895588Lot Number: 7390 ; 8) SNE69PSKR4, UDI-DI: 10197106895580(each), 50197106895588(case) 8 1019710697900650197106979004Lot Number: 13673 ; 9) SNE7CSHY15, UDI-DI: 10197106979006(each), 50197106979004(case) 9 1019895602658250198956026580Lot Number: 13673 ; 10) SNE7CSHY16, UDI-DI: 10198956026582(each), 50198956026580(case) 10 1019710670559950197106705597Lot Number: 14813 ; 11) SOP30ODSCL, UDI-DI: 10197106705599(each), 50197106705597(case) 11 Lot Number: 14813 - Amount recalled
- 602 kits
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
- Nationwide
Why it was recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
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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