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
12 of 12 products
| Model / number | Product as published |
|---|---|
| — | KIT, LAP CHOLE , Catalog Number: PGCGLCBAC |
| — | KIT, LAP CHOLE , Catalog Number: PGCGLCBAD |
| — | KIT, LAP CHOLE , Catalog Number: PGCGLCBAE |
PGCGLCB11 | KIT, LAP CHOLE |
PV63CMST5 | KIT, CARDIO MINIMALLY INVASIVE |
SBA23RBHNG | HMC ROBOTIC PACK |
SBA23RBHNH | HMC ROBOTIC PACK |
SBA30EDCLB | ENS ENDOCHOLEYCYSTECTOMIE 4 |
SLC37LCJOB | LAP CHOLE PACK |
SLC37LCJ21 | LAP CHOLE PACK |
SLC37LCJ22 | LAP CHOLE PACK |
SMA30RBHSA | PACK GYNE ROBOTIC |
- Lot codes and dates
57 of 57 products
Products covered by this recall # Barcodes Product as published 1 1019710675174950197106751747Lot Number: 24309FG2 ; 2) PGCGLCBAC, UDI-DI: 10197106751749(each), 50197106751747(case) 2 1019710675174950197106751747Lot Number: 24352FG2 ; 3) PGCGLCBAC, UDI-DI: 10197106751749(each), 50197106751747(case) 3 1019710675174950197106751747Lot Number: 24317FG2 ; 4) PGCGLCBAC, UDI-DI: 10197106751749(each), 50197106751747(case) 4 1019895623030950198956230307Lot Number: 25062FG2 ; 5) PGCGLCBAD, UDI-DI: 10198956230309(each), 50198956230307(case) 5 1019895623030950198956230307Lot Number: 25121FG2 ; 6) PGCGLCBAD, UDI-DI: 10198956230309(each), 50198956230307(case) 6 1019895636336650198956363364Lot Number: 25045FG2 ; 7) PGCGLCBAE, UDI-DI: 10198956363366(each), 50198956363364(case) 7 1019895611617750198956116175Lot Number: 25217FG2 ; 8) PGCGLCB11, UDI-DI: 10198956116177(each), 50198956116175(case) 8 1019895652620450198956526202Lot Number: 24355FG2 ; 9) PV63CMST5, UDI-DI: 10198956526204(each), 50198956526202(case) 9 1019710641757750197106417575Lot Number: 25148FG2 ; 10) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 10 1019710641757750197106417575Lot Number: 24317FG2 ; 11) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 11 1019710641757750197106417575Lot Number: 24325FG2 ; 12) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 12 1019710641757750197106417575Lot Number: 24317FG2 ; 13) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 13 1019710641757750197106417575Lot Number: 25029FG2 ; 14) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 14 1019710641757750197106417575Lot Number: 25069FG2 ; 15) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 15 1019710641757750197106417575Lot Number: 25045FG2 ; 16) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 16 1019710641757750197106417575Lot Number: 25069FG2 ; 17) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 17 1019710641757750197106417575Lot Number: 24317FG2 ; 18) SBA23RBHNG, UDI-DI: 10197106417577(each), 50197106417575(case) 18 1019895633201050198956332018Lot Number: 25085FG2 ; 19) SBA23RBHNH, UDI-DI: 10198956332010(each), 50198956332018(case) 19 1019895628695550198956286953Lot Number: 25217FG2 ; 20) SBA30EDCLB, UDI-DI: 10198956286955(each), 50198956286953(case) 20 1019895628695550198956286953Lot Number: 25217FG2 ; 21) SBA30EDCLB, UDI-DI: 10198956286955(each), 50198956286953(case) - Amount recalled
- 3677 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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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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