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
PWV2MF104KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF105KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF106KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF107KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF108KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF109KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF10VKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF10WKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF10YKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF10ZKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF111KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MF112KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MFCP2KIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MFCP3KIT,MAXILLOFACIAL PRESBYTERIAN
PWV2MFCP4KIT,MAXILLOFACIAL PRESBYTERIAN
PWV2MFCPAKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MFCPBKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MFCPCKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MFCPDKIT,MAXILLOFACIAL,PRESBYTERIAN
PWV2MFCPEKIT,MAXILLOFACIAL PRESBYTERIAN
Lot codes and dates

35 of 35 products

Products covered by this recall
#BarcodesProduct as published
11088843967616750888439676165PWV2MF104, UDI-DI:10888439676167 (each) 50888439676165 (case), Lot Number: J46C10
21019559400421750195594004215PWV2MF105, UDI-DI:10195594004217 (each) 50195594004215 (case), Lot Number: J8998R
31019559409599450195594095992PWV2MF106, UDI-DI:10195594095994 (each) 50195594095992 (case), Lot Number: 5136000
41019559414806550195594148063PWV2MF107, UDI-DI:10195594148065 (each) 50195594148063 (case), Lot Number: 5140389
51019559422894150195594228949PWV2MF108, UDI-DI:10195594228941 (each) 50195594228949 (case), Lot Number: 5140389
61019559439487550195594394873PWV2MF109, UDI-DI:10195594394875 (each) 50195594394873 (case), Lot Number: J65K18
71088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: HP1027
81088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: J4220A
91088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: J43W15
101088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: J4953C
111088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: J6022K
121088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: J6372Z
131088843934274150888439342749PWV2MF10V, UDI-DI:10888439342741 (each) 50888439342749 (case), Lot Number: J7708T
141088843969364550888439693643PWV2MF10W, UDI-DI:10888439693645 (each) 50888439693643 (case), Lot Number: J8241D
151088843996743250888439967430PWV2MF10Y, UDI-DI:10888439967432 (each) 50888439967430 (case), Lot Number: J84K11
161088843996743250888439967430PWV2MF10Y, UDI-DI:10888439967432 (each) 50888439967430 (case), Lot Number: J84K10
171019559418029450195594180292PWV2MF10Z, UDI-DI:10195594180294 (each) 50195594180292 (case), Lot Number: J65K19
181019559418029450195594180292PWV2MF10Z, UDI-DI:10195594180294 (each) 50195594180292 (case), Lot Number: 5775812
191019559418029450195594180292PWV2MF10Z, UDI-DI:10195594180294 (each) 50195594180292 (case), Lot Number: 6116189
201019559418029450195594180292PWV2MF10Z, UDI-DI:10195594180294 (each) 50195594180292 (case), Lot Number: 6251076
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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By hazard

Other recalls from Cardinal Health 200, LLC

54 in total.

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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, 5:41 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.