Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC2C; 4) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC2D; 5) CHI STD NEURO CRANI OPT 4 , Catalog Number: CHIP99NC2D; 6) KIT, IUS NASAL , Catalog Number: PECGNSBOA; 7) KIT,NASAL FENS, SW , Catalog Number: PEMHNFMHB; 8) KIT,ENT , Catalog Number: PEMIEPHP2; 9) KIT,ENT , Catalog Number: PEMIEPHP3; 10) KIT,ENT , Catalog Number: PEMIEPHPB; 11) KIT, NASAL SINUS P, Catalog Number: PEV2CL016; 12) KIT, ENT FESS , Catalog Number: PEV2FSNYC;

Class II

Recalling firm: Cardinal Health 200, LLC
Reason for recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Affected products (lot / model / serial): 3790) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 4730 ; 3791) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 2221315564 ; 3792) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 338058 ; 3793) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 4869 ; 3794) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 7784 ; 3795) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 7784 ; 3796) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 7784 ; 3797) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 7784 ; 3798) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 7784 ; 3799) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 9243-1 ; 3800) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 3024-2 ; 3801) SNE30CNRCD, UDI-DI: 10195594687052(each), 50195594687050(case), Lot Number: 3916-2 ; 3802) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 9243 ; 3803) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 9243-2 ; 3804) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 9243-2 ; 3805) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 11020 ; 3806) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 11020 ; 3807) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 11020 ; 3808) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 10586 ; 3809) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 14813 ; 3810) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15192-1 ; 3811) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15463 ; 3812) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15463-6 ; 3813) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15463-7 ; 3814) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 6865 ; 3815) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 9243-1 ; 3816) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 10339 ; 3817) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 9243-1 ; 3818) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 11020 ; 3819) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 11020 ; 3820) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 10586 ; 3821) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15192 ; 3822) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15192 ; 3823) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15463 ; 3824) SNE30CNRCE, UDI-DI: 10197106605233(each), 50197106605231(case), Lot Number: 15463-3 ; 3825) SNE3
Units affected: 401311 kits
Distribution pattern: US Nationwide. Canada.
Firm location: Waukegan, IL, United States
Recall type: Voluntary: Firm initiated
How the firm notified customers: Letter
Product type: Devices
Status: Ongoing
Recall number: Z-2947-2026
Recall initiated: July 14, 2026
FDA classification date: August 13, 2026
FDA report date: August 19, 2026
FDA event ID: 99380
Last updated on HTM Vibe: August 26, 2026

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