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
38 of 38 products
| Model / number | Product as published |
|---|---|
21-4720B | FAT GRAFT ADD KIT |
21-4720C | TRAY FAT GRAFT ADD |
| — | KIT,BOSC MICROLARYNGOSCOPY , Catalog Number: PECGMLBOB |
PECGNAAU8 | KIT,ASLMC NASAL PACK |
PECGNAAU8 | KIT,ASLMC NASAL PACK |
PN1DTSLH9 | KIT, TRIPOINT SPINE |
PN1DTSLHC | KIT, TRIPOINT SPINE |
PN1DTSLHD | KIT, TRIPOINT SPINE |
PN1DTSLHE | KIT, TRIPOINT SPINE |
PN21OTMC6 | KIT,NEURO |
PN21OTMC7 | KIT,NEURO |
PN21OTMCC | KIT,NEURO |
PN21OTMCD | KIT,NEURO |
PN33CRMYB | KIT, MER CRANI |
PN36NBCHB | KIT,CHP BASIC NEURO |
PN40CKC27 | KIT, CRANIOTOMY |
PN40CKC28 | KIT, CRANIOTOMY |
PN40CKC29 | KIT, CRANIOTOMY |
PN40CKCFC | KIT, CRANIOTOMY |
| — | KIT, BAL LUMBAR LAMINECTOMY , Catalog Number: PNCGLLBMB |
- Lot codes and dates
396 of 396 products
Products covered by this recall Model / number Barcodes Product as published — 1019710667579350197106675791Lot Number: 94970 ; 2) 21-4720C, UDI-DI: 10197106675793(each), 50197106675791(case) — 1019710667579350197106675791Lot Number: 10339 ; 3) 21-4720C, UDI-DI: 10197106675793(each), 50197106675791(case) — 1019710606740650197106067404Lot Number: 10586 ; 4) PECGMLBOB, UDI-DI: 10197106067406(each), 50197106067404(case) — 1019710696770650197106967704Lot Number: 4366 ; 5) PECGNAAU8, UDI-DI: 10197106967706(each), 50197106967704(case) — 1019710689451450197106894512Lot Number: 12206 ; 6) PECGNAAUJ, UDI-DI: 10197106894514(each), 50197106894512(case) — Lot Number: 11851 ; 7) 1DTSLH91019895612005150198956120059UDI-DI: 10198956120051(each), 50198956120059(case) — Lot Number: 14813 ; 8) 1DTSLH91019895612005150198956120059UDI-DI: 10198956120051(each), 50198956120059(case) — Lot Number: 14039 ; 9) 1DTSLHC1019710649222250197106492220UDI-DI: 10197106492222(each), 50197106492220(case) — Lot Number: 8160-1 ; 10) 1DTSLHC1019710649222250197106492220UDI-DI: 10197106492222(each), 50197106492220(case) — Lot Number: 3747 ; 11) 1DTSLHD1019710666019550197106660193UDI-DI: 10197106660195(each), 50197106660193(case) — Lot Number: 10392 ; 12) 1DTSLHD1019710666019550197106660193UDI-DI: 10197106660195(each), 50197106660193(case) — Lot Number: 10392 ; 13) 1DTSLHD1019710666019550197106660193UDI-DI: 10197106660195(each), 50197106660193(case) — Lot Number: 11020 ; 14) - Amount recalled
- 36862 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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