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
12 of 12 products
| Model / number | Product as published |
|---|---|
CHIP99NC27 | CHI STD NEURO CRANI OPT 2 |
CHIP99NC28 | CHI STD NEURO CRANI OPT 2 |
CHIP99NC2C | CHI STD NEURO CRANI OPT 2 |
CHIP99NC2D | CHI STD NEURO CRANI OPT 2 |
CHIP99NC2D | CHI STD NEURO CRANI OPT 4 |
| — | KIT, IUS NASAL , Catalog Number: PECGNSBOA |
| — | KIT,NASAL FENS, SW , Catalog Number: PEMHNFMHB |
PEMIEPHP2 | KIT,ENT |
PEMIEPHP3 | KIT,ENT |
| — | KIT,ENT , Catalog Number: PEMIEPHPB |
PEV2CL016 | KIT, NASAL SINUS P |
PEV2FSNYC | KIT, ENT FESS |
- Lot codes and dates
286 of 286 products
Products covered by this recall # Barcodes Product as published 1 1019559468705250195594687050Lot Number: 4730 ; 3791) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 2 1019559468705250195594687050Lot Number: 2221315564 ; 3792) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 3 1019559468705250195594687050Lot Number: 338058 ; 3793) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 4 1019559468705250195594687050Lot Number: 4869 ; 3794) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 5 1019559468705250195594687050Lot Number: 7784 ; 3795) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 6 1019559468705250195594687050Lot Number: 7784 ; 3796) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 7 1019559468705250195594687050Lot Number: 7784 ; 3797) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 8 1019559468705250195594687050Lot Number: 7784 ; 3798) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 9 1019559468705250195594687050Lot Number: 7784 ; 3799) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 10 1019559468705250195594687050Lot Number: 9243-1 ; 3800) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 11 1019559468705250195594687050Lot Number: 3024-2 ; 3801) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case) 12 1019710660523350197106605231Lot Number: 3916-2 ; 3802) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 13 1019710660523350197106605231Lot Number: 9243 ; 3803) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 14 1019710660523350197106605231Lot Number: 9243-2 ; 3804) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 15 1019710660523350197106605231Lot Number: 9243-2 ; 3805) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 16 1019710660523350197106605231Lot Number: 11020 ; 3806) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 17 1019710660523350197106605231Lot Number: 11020 ; 3807) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 18 1019710660523350197106605231Lot Number: 11020 ; 3808) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 19 1019710660523350197106605231Lot Number: 10586 ; 3809) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) 20 1019710660523350197106605231Lot Number: 14813 ; 3810) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case) - Amount recalled
- 401311 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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