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

Products covered by this recall
Model / numberProduct as published
SEN73NSKCFSEPTO RHINO PACK
SNE30CNOHEPACK NEURO MINOR CRANIOTOMY
SNE30CRJGYNEURO MAJOR 2 PACK
SNE43NEE13NEURO PACK
SNE43NEE13LAMINECTOMY PACK
SNE5CLPB13LAMINECTOMY PACK
SNE69PSKR4PEDI SPINE R
SNE7CSHY15SHUNT PACK
SNE7CSHY16SHUNT PACK
SOP30ODSCLENS ORTHO FUSION POSTERIEURE 3
Lot codes and dates

11 of 11 products

Products covered by this recall
#BarcodesProduct as published
11019559450623050195594506238Lot Number: 3024-2 ; 2) SNE30CNOHE, UDI-DI: 10195594506230(each), 50195594506238(case)
21019559445399250195594453990Lot Number: 93845 ; 3) SNE30CRJGY, UDI-DI: 10195594453992(each), 50195594453990(case)
31019895647096550198956470963Lot Number: 4730 ; 4) SNE43NEE13, UDI-DI: 10198956470965(each), 50198956470963(case)
41019710626668750197106266685Lot Number: 14039 ; 5) SNE5CLPB12, UDI-DI: 10197106266687(each), 50197106266685(case)
51019710626668750197106266685Lot Number: 6033 ; 6) SNE5CLPB12, UDI-DI: 10197106266687(each), 50197106266685(case)
61019710632813250197106328130Lot Number: 4366 ; 7) SNE5CLPB13, UDI-DI: 10197106328132(each), 50197106328130(case)
71019710689558050197106895588Lot Number: 7390 ; 8) SNE69PSKR4, UDI-DI: 10197106895580(each), 50197106895588(case)
81019710697900650197106979004Lot Number: 13673 ; 9) SNE7CSHY15, UDI-DI: 10197106979006(each), 50197106979004(case)
91019895602658250198956026580Lot Number: 13673 ; 10) SNE7CSHY16, UDI-DI: 10198956026582(each), 50198956026580(case)
101019710670559950197106705597Lot Number: 14813 ; 11) SOP30ODSCL, UDI-DI: 10197106705599(each), 50197106705597(case)
11Lot 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.

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.

Free recall alerts

Get alerted about new Cardinal Health 200, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:15 PM 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.