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

21 of 21 products

Products covered by this recall
Model / numberProduct as published
PVV20110BKIT, CAROTID ENDARTERECTOMY
PVV20110DKIT, CAROTID ENDARTERECTOMY
PVV2CA103KIT,CAROTID ENDARTERECTOMY
PVV2CA10TKIT,CAROTID ENDARTERECTOMY
PVV2CA10UKIT,CAROTID ENDARTERECTOMY
PVV2CA10XKIT, CAROTID ENDARTERECTOMY
PVV2CA10YKIT, CAROTID ENDARTERECTOMY
SCV13AASLASLH AAA PACK
SCV30VAF10CALGARY MICROVASCULAR FREEFLAP
SCV30VAFH4CALGARY MICROVASCULAR FREEFLAP
SCV30VAFH5CALGARY MICROVASCULAR FREEFLAP
SCV30VAFH6CALGARY MICROVASCULAR FREEFLAP
SCV30VAFH7CALGARY MICROVASCULAR FREEFLAP
SCV30VAFH8CALGARY MICROVASCULAR FREEFLAP
SCV30VAFH9CALGARY MICROVASCULAR FREEFLAP
SCV30VAFHPMICROVASCULAR FREE FLAP
SCV30VAFHQMICROVASCULAR FREE FLAP
SCV30VAFHRCALGARY MICROVASCULAR FREEFLAP
SCV30VAFHSCALGARY MICROVASCULAR FREEFLAP
SNE11AN102NEURO EMBOLISM PACK
Lot codes and dates

60 of 60 products

Products covered by this recall
#BarcodesProduct as published
11019710629141250197106291410PVV20110B, UDI-DI:10197106291412 (each) 50197106291410 (case), Lot Number: 6788690
21019710629141250197106291410PVV20110B, UDI-DI:10197106291412 (each) 50197106291410 (case), Lot Number: 6806122
31019710629141250197106291410PVV20110B, UDI-DI:10197106291412 (each) 50197106291410 (case), Lot Number: 7160517
41019710654650550197106546503PVV20110D, UDI-DI:10197106546505 (each) 50197106546503 (case), Lot Number: 7287574
51088843971408150888439714089PVV2CA103, UDI-DI:10888439714081 (each) 50888439714089 (case), Lot Number: J46C12
61088843934946750888439349465PVV2CA10T, UDI-DI:10888439349467 (each) 50888439349465 (case), Lot Number: J46C11
71088843934946750888439349465PVV2CA10T, UDI-DI:10888439349467 (each) 50888439349465 (case), Lot Number: J43W16
81088843934946750888439349465PVV2CA10T, UDI-DI:10888439349467 (each) 50888439349465 (case), Lot Number: J6022K
91088843934946750888439349465PVV2CA10T, UDI-DI:10888439349467 (each) 50888439349465 (case), Lot Number: J7708R
101088843934946750888439349465PVV2CA10T, UDI-DI:10888439349467 (each) 50888439349465 (case), Lot Number: J79Z50
111088843969360750888439693605PVV2CA10U, UDI-DI:10888439693607 (each) 50888439693605 (case), Lot Number: J8241D
121088843969360750888439693605PVV2CA10U, UDI-DI:10888439693607 (each) 50888439693605 (case), Lot Number: J84K11
131088843996726550888439967263PVV2CA10X, UDI-DI:10888439967265 (each) 50888439967263 (case), Lot Number: J8998R
141019559417579550195594175793PVV2CA10Y, UDI-DI:10195594175795 (each) 50195594175793 (case), Lot Number: 5140389
151019559417579550195594175793PVV2CA10Y, UDI-DI:10195594175795 (each) 50195594175793 (case), Lot Number: 5664115
161019559417579550195594175793PVV2CA10Y, UDI-DI:10195594175795 (each) 50195594175793 (case), Lot Number: 5858468
171019559417579550195594175793PVV2CA10Y, UDI-DI:10195594175795 (each) 50195594175793 (case), Lot Number: 5858469
181019559417579550195594175793PVV2CA10Y, UDI-DI:10195594175795 (each) 50195594175793 (case), Lot Number: 6116189
191019559417579550195594175793PVV2CA10Y, UDI-DI:10195594175795 (each) 50195594175793 (case), Lot Number: 6251075
201019710651448150197106514489SCV13AASLA, UDI-DI:10197106514481 (each) 50197106514489 (case), Lot Number: 7055826
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, 5:38 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.