Reported Oct 7, 2026 · Ongoing · Updated Oct 13, 2026
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets
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?
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets
8 of 8 products
| Model / number | Product as published |
|---|---|
| — | KIT,GU DAVINCI , Catalog Number: PGVMDVBWU |
| — | KIT,GU DAVINCI , Catalog Number: PGVMDVBWV |
PGVMDVB26 | KIT,GU DAVINCI |
PGVMDVB27 | KIT,GU DAVINCI |
PGVMDVB28 | KIT,GU DAVINCI |
PGVMDVB29 | KIT,GU DAVINCI |
SBA73CLKFD | COLORECTAL PACK |
SBA73CLK26 | COLORECTAL PACK |
- Lot codes and dates
18 of 18 products
Products covered by this recall # Barcodes Product as published 1 1088843962618650888439626184Lot Number: 24317FG2 ; 2) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case) 2 1088843962618650888439626184Lot Number: 24353FG2 ; 3) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case) 3 1088843962618650888439626184Lot Number: 24317FG2 ; 4) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case) 4 1088843962618650888439626184Lot Number: 25069FG2 ; 5) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case) 5 1088843962618650888439626184Lot Number: 25045FG2 ; 6) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case) 6 1019895620403450198956204032Lot Number: 25069FG2 ; 7) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case) 7 1019895620403450198956204032Lot Number: 24353FG2 ; 8) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case) 8 1019895620403450198956204032Lot Number: 25101FG2 ; 9) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case) 9 1019895620403450198956204032Lot Number: 25148FG2 ; 10) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case) 10 1019895600779650198956007794Lot Number: 25217FG2 ; 11) PGVMDVB26, UDI-DI: 10198956007796(each), 50198956007794(case) 11 1019895605471450198956054712Lot Number: 24309FG2 ; 12) PGVMDVB27, UDI-DI: 10198956054714(each), 50198956054712(case) 12 1019895607984750198956079845Lot Number: 24325FG2 ; 13) PGVMDVB28, UDI-DI: 10198956079847(each), 50198956079845(case) 13 1019895607984750198956079845Lot Number: 24317FG2 ; 14) PGVMDVB28, UDI-DI: 10198956079847(each), 50198956079845(case) 14 1019895609402450198956094022Lot Number: 24325FG2 ; 15) PGVMDVB29, UDI-DI: 10198956094024(each), 50198956094022(case) 15 1019895609402450198956094022Lot Number: 24317FG2 ; 16) PGVMDVB29, UDI-DI: 10198956094024(each), 50198956094022(case) 16 1019710663396050197106633968Lot Number: 24348FG2 ; 17) SBA73CLKFD, UDI-DI: 10197106633960(each), 50197106633968(case) 17 1019895602982850198956029826Lot Number: 25055FG2 ; 18) SBA73CLK26, UDI-DI: 10198956029828(each), 50198956029826(case) 18 Lot Number: 24309FG2 - Amount recalled
- 344 kits
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.
This product could cause temporary or reversible health problems — stop using it.
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