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

76 of 76 products

Products covered by this recall
Model / numberProduct as published
PE29NSFG4KIT,NASAL SEPTOPLASTY,FAIRVIEW
PE29NSFG5KIT,NASAL SEPTOPLASTY,FAIRVIEW
PE29NSFG6KIT,NASAL SEPTOPLASTY,FAIRVIEW
PE29NSFG7KIT,NASAL SEPTOPLASTY,FAIRVIEW
PE29NSFG8KIT,NASAL SEPTOPLASTY,FAIRVIEW
PE29NSFGMKIT,NASAL SEPTOPLASTY,FAIRVIEW
PE29NSFGNKIT,NASAL SEPTOPLASTY,FAIRVIEW
PE36ESCHAKIT,CHP SINUS ENDOSCOPY
PECGOTSN1KIT, SSSC ENT
PECGOTSN2KIT, SSSC ENT
PECGOTSN3KIT, SSSC ENT
KIT, SSSC ENT, Catalog Number:PECGOTSNA
KIT, SSSC ENT, Catalog Number:PECGOTSNB
KIT, SSSC ENT, Catalog Number:PECGOTSNC
KIT, SSSC ENT, Catalog Number:PECGOTSND
KIT, SSSC ENT, Catalog Number:PECGOTSNE
PEV2EA10OKIT,MAJOR EAR,PRESBYTERIAN
PEV2EA10PKIT,MAJOR EAR,PRESBYTERIAN
PEV2EA10QKIT,MAJOR EAR,PRESBYTERIAN
PEV2EA10RKIT,MAJOR EAR,PRESBYTERIAN
Lot codes and dates

329 of 329 products

Products covered by this recall
#BarcodesProduct as published
11019559430287050195594302878PE29NSFG4, UDI-DI:10195594302870 (each) 50195594302878 (case), Lot Number: 5140385
21019559442998050195594429988PE29NSFG5, UDI-DI:10195594429980 (each) 50195594429988 (case), Lot Number: 5478805
31019559451004650195594510044PE29NSFG6, UDI-DI:10195594510046 (each) 50195594510044 (case), Lot Number: 5664108
41019710651120650197106511204PE29NSFG7, UDI-DI:10197106511206 (each) 50197106511204 (case), Lot Number: 7280115
51019710653598150197106535989PE29NSFG8, UDI-DI:10197106535981 (each) 50197106535989 (case), Lot Number: 7320240
61088542555463850885425554636PE29NSFGM, UDI-DI:10885425554638 (each) 50885425554636 (case), Lot Number: J3593N
71088542555463850885425554636PE29NSFGM, UDI-DI:10885425554638 (each) 50885425554636 (case), Lot Number: J46C07
81088542555463850885425554636PE29NSFGM, UDI-DI:10885425554638 (each) 50885425554636 (case), Lot Number: J4952P
91088542555463850885425554636PE29NSFGM, UDI-DI:10885425554638 (each) 50885425554636 (case), Lot Number: J5679N
101088542555463850885425554636PE29NSFGM, UDI-DI:10885425554638 (each) 50885425554636 (case), Lot Number: J5679T
111088542555463850885425554636PE29NSFGM, UDI-DI:10885425554638 (each) 50885425554636 (case), Lot Number: J7905H
121088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: 6701854
131088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: 7005491
141088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: 7266056
151088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: 7280114
161088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: J84K06
171088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: J8693H
181088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: J8693K
191088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: J6368Z
201088843989331150888439893319PE29NSFGN, UDI-DI:10888439893311 (each) 50888439893319 (case), Lot Number: J9197H
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, 6:57 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.