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
10 of 10 products
| Model / number | Product as published |
|---|---|
PB23GLNLAC | KIT, GYN LAPAROSCOPY NEW HAN |
PB23GLNLA1 | KIT, GYN LAPAROSCOPY NEW HAN |
PB23GLNLA2 | KIT, GYN LAPAROSCOPY NEW HAN |
PB23GLNLA3 | KIT, GYN LAPAROSCOPY NEW HAN |
PB23GLNLA4 | KIT, GYN LAPAROSCOPY NEW HAN |
PB23GRNLD | KIT, GYN ROBOTIC NEW HAN |
PB23GRNLE | KIT, GYN ROBOTIC NEW HAN |
PB23GRNL5 | KIT, GYN ROBOTIC NEW HAN |
PB23GRNL6 | KIT, GYN ROBOTIC NEW HAN |
| — | MVHS GU GYN ROBOT PACK , Catalog Number: SOTDKGREFB |
- Lot codes and dates
33 of 33 products
Products covered by this recall # Barcodes Product as published 1 1019710676090150197106760909Lot Number: 24317FG2 ; 2) PB23GLNLAC, UDI-DI: 10197106760901(each), 50197106760909(case) 2 1019710676090150197106760909Lot Number: 24347FG2 ; 3) PB23GLNLAC, UDI-DI: 10197106760901(each), 50197106760909(case) 3 1019710676090150197106760909Lot Number: 24355FG2 ; 4) PB23GLNLAC, UDI-DI: 10197106760901(each), 50197106760909(case) 4 1019710676090150197106760909Lot Number: 25069FG2 ; 5) PB23GLNLAC, UDI-DI: 10197106760901(each), 50197106760909(case) 5 1019710676090150197106760909Lot Number: 25014FG2 ; 6) PB23GLNLAC, UDI-DI: 10197106760901(each), 50197106760909(case) 6 1019710680996950197106809967Lot Number: 25029FG2 ; 7) PB23GLNLA1, UDI-DI: 10197106809969(each), 50197106809967(case) 7 1019895605332850198956053326Lot Number: 20 ; 8) PB23GLNLA2, UDI-DI: 10198956053328(each), 50198956053326(case) 8 1019895606684750198956066845Lot Number: 24317FG2 ; 9) PB23GLNLA3, UDI-DI: 10198956066847(each), 50198956066845(case) 9 1019895606684750198956066845Lot Number: 24309FG2 ; 10) PB23GLNLA3, UDI-DI: 10198956066847(each), 50198956066845(case) 10 1019895606684750198956066845Lot Number: 24317FG2 ; 11) PB23GLNLA3, UDI-DI: 10198956066847(each), 50198956066845(case) 11 1019895607266450198956072662Lot Number: 24325FG2 ; 12) PB23GLNLA4, UDI-DI: 10198956072664(each), 50198956072662(case) 12 1019895607266450198956072662Lot Number: 24317FG2 ; 13) PB23GLNLA4, UDI-DI: 10198956072664(each), 50198956072662(case) 13 1019710696896350197106968961Lot Number: 24325FG2 ; 14) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 14 1019710696896350197106968961Lot Number: 24353FG2 ; 15) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 15 1019710696896350197106968961Lot Number: 24355FG2 ; 16) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 16 1019710696896350197106968961Lot Number: 24317FG2 ; 17) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 17 1019710696896350197106968961Lot Number: 24353FG2 ; 18) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 18 1019710696896350197106968961Lot Number: 24353FG2 ; 19) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 19 1019710696896350197106968961Lot Number: 25029FG2 ; 20) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) 20 1019710696896350197106968961Lot Number: 25045FG2 ; 21) PB23GRNLD, UDI-DI: 10197106968963(each), 50197106968961(case) - Amount recalled
- 2957 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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