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
15 of 15 products
| Model / number | Product as published |
|---|---|
PN33NBMYD | KIT, MER NEURO BACK |
PN36NBCH4 | KIT,CHP BASIC NEURO |
PN36NBCH5 | KIT,CHP BASIC NEURO |
PN41ACLA9 | KIT, ANT CERVICAL DISC |
PN41ACLA9 | KIT, ANT CERVICAL DISC |
PN41ACLAI | KIT, ANT CERVICAL DISC |
PN41LMB10 | KIT, LAMINECTOMY |
PN41LMB11 | KIT, LAMINECTOMY |
PN41LMB12 | KIT, LAMINECTOMY |
PN41LMBLC | KIT, NEURO LAMINECTOMY |
| — | KIT, BAL CRANIOTOMY , Catalog Number: PNCGCRBMF |
| — | KIT,LAMINECTOMY NH , Catalog Number: PNOCLNNHB |
PNVMOTA235 | KIT, NEURO LAMINECTOMY |
PNVMOTA236 | KIT, NEURO LAMINECTOMY |
PNVMOTA237 | KIT, NEURO LAMINECTOMY , ; 63 |
- Lot codes and dates
292 of 292 products
Products covered by this recall Model / number Barcodes Product as published 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 15463-6 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 15463-6 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 14039 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 14039 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 14813 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 15192 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 15192 33NBMYD1019895618747450198956187472UDI-DI: 10198956187474(each), 50198956187472(case), Lot Number: 15192 36NBCH41019895612986350198956129861UDI-DI: 10198956129863(each), 50198956129861(case), Lot Number: 14813 36NBCH51019895613153850198956131536UDI-DI: 10198956131538(each), 50198956131536(case), Lot Number: 14813 41ACLA91019710634610550197106346103UDI-DI: 10197106346105(each), 50197106346103(case), Lot Number: 4869 41ACLAH1019559417730050195594177308UDI-DI: 10195594177300(each), 50195594177308(case), Lot Number: 4366 41ACLAH1019559417730050195594177308UDI-DI: 10195594177300(each), 50195594177308(case), Lot Number: 4366 41ACLAH1019559417730050195594177308UDI-DI: 10195594177300(each), 50195594177308(case), Lot Number: 1726-1 41ACLAH1019559417730050195594177308UDI-DI: 10195594177300(each), 50195594177308(case), Lot Number: 1726-1 41ACLAH1019559417730050195594177308UDI-DI: 10195594177300(each), 50195594177308(case), Lot Number: 3024 41ACLAH1019559417730050195594177308UDI-DI: 10195594177300(each), 50195594177308(case), Lot Number: 3916-1 41ACLAI1019710632081550197106320813UDI-DI: 10197106320815(each), 50197106320813(case), Lot Number: 7748 41ACLAI1019710632081550197106320813UDI-DI: 10197106320815(each), 50197106320813(case), Lot Number: 8160 41ACLAI1019710632081550197106320813UDI-DI: 10197106320815(each), 50197106320813(case), Lot Number: 8160 - Amount recalled
- 52699 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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