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

Products covered by this recall
Model / numberProduct as published
PN33NBMYDKIT, MER NEURO BACK
PN36NBCH4KIT,CHP BASIC NEURO
PN36NBCH5KIT,CHP BASIC NEURO
PN41ACLA9KIT, ANT CERVICAL DISC
PN41ACLA9KIT, ANT CERVICAL DISC
PN41ACLAIKIT, ANT CERVICAL DISC
PN41LMB10KIT, LAMINECTOMY
PN41LMB11KIT, LAMINECTOMY
PN41LMB12KIT, LAMINECTOMY
PN41LMBLCKIT, NEURO LAMINECTOMY
KIT, BAL CRANIOTOMY , Catalog Number: PNCGCRBMF
KIT,LAMINECTOMY NH , Catalog Number: PNOCLNNHB
PNVMOTA235KIT, NEURO LAMINECTOMY
PNVMOTA236KIT, NEURO LAMINECTOMY
PNVMOTA237KIT, NEURO LAMINECTOMY , ; 63
Lot codes and dates

292 of 292 products

Products covered by this recall
Model / numberBarcodesProduct 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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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.