Reported Feb 19, 2025 · Ongoing

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

83 of 83 products

Products covered by this recall
Model / numberProduct as published
CHIP99NC12CHI STD NEURO CRANI OPT 1
CHIP99NC13CHI STD NEURO CRANI OPT 1
CHIP99NC14CHI STD NEURO CRANI OPT 1
CHIP99NC15CHI STD NEURO CRANI OPT 1
CHIP99NC16CHI STD NEURO CRANI OPT 1
CHIP99NC17CHI STD NEURO CRANI OPT 1
CHIP99NC18CHI STD NEURO CRANI OPT 1
CHIP99NC1DCHI STD NEURO CRANI OPT 1
CHIP99NC22CHI STD NEURO CRANI OPT 2
CHIP99NC23CHI STD NEURO CRANI OPT 2
CHIP99NC24CHI STD NEURO CRANI OPT 2
CHIP99NC25CHI STD NEURO CRANI OPT 2
CHIP99NC26CHI STD NEURO CRANI OPT 2
CHIP99NC2CCHI STD NEURO CRANI OPT 2
CHIP99SP32CHI STD SPINE OPTION 3
CHIP99SP33CHI STD SPINE OPTION 3
CHIP99SP34CHI STD SPINE OPTION 3
CHIP99SP3DCHI STD SPINE OPTION 3
P55VNVP09AKIT, VP SHUNT
KIT,ANT CERVICAL DISK,MO BAP, Catalog Number:PGVMACMOQ
Lot codes and dates

330 of 330 products

Products covered by this recall
Model / numberBarcodesProduct as published
1019559410547150195594105479CHIP99NC12, UDI-DI:10195594105471 (each) 50195594105479 (case), Lot Number: J8692J
1019559420237850195594202376CHIP99NC13, UDI-DI:10195594202378 (each) 50195594202376 (case), Lot Number: 5138245
1019559427689850195594276896CHIP99NC14, UDI-DI:10195594276898 (each) 50195594276896 (case), Lot Number: 5324036
1019559439969650195594399694CHIP99NC15, UDI-DI:10195594399696 (each) 50195594399694 (case), Lot Number: 5530905
1019559444484650195594444844CHIP99NC16, UDI-DI:10195594444846 (each) 50195594444844 (case), Lot Number: 5530911
1019710604615950197106046157CHIP99NC17, UDI-DI:10197106046159 (each) 50197106046157 (case), Lot Number: 6560930
1019710616964350197106169641CHIP99NC18, UDI-DI:10197106169643 (each) 50197106169641 (case), Lot Number: 6701892
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: 6264447
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: 6986972
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: 7005424
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J4218Z
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J4678H
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J4678T
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J4950P
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J53W06
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: N/A
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J6049N
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J6365Y
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J77Z27
1088843900795450888439007952CHIP99NC1D, UDI-DI:10888439007954 (each) 50888439007952 (case), Lot Number: J82M02
Amount recalled
973,785 total units

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

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.

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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, 7:11 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.