Cardinal Health 200 Presource Packs Containing Stryker StrykeFlow PS and AHTO Tube Sets
The tube sets may leak fluid during use, potentially causing a slip and fall.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Cardinal Health 200, LLC recalled Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets because the tube sets may leak during use, with fluid pooling on the floor, potentially causing a slip and fall. The recall began August 18, 2026, and was added to the FDA's Enforcement Report on September 25, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the list below, then check the codes the FDA notice also names.
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets
- UDI-DI
- 10197106980866
- 50197106980864
- Lot
- 25069FG2
- 25101FG2
- UDI-DI
- 10888439626186
- 50888439626184
- 10198956204034
- 50198956204032
- Lot
- 24317FG2
- 24353FG2
- 25069FG2
- 25045FG2
- 25101FG2
- 25148FG2
- 25217FG2
- 24309FG2
- 24325FG2
- 24348FG2
- 25055FG2
- UDI-DI
- 10197106751749
- 50197106751747
- 10198956230309
- 50198956230307
- 10198956363366
- 50198956363364
- 10198956116177
- 50198956116175
- 10198956526204
- 50198956526202
- 10197106417577
- 50197106417575
- Lot
- 24309FG2
- 24352FG2
- 24317FG2
- 25062FG2
- 25121FG2
- 25045FG2
- 25217FG2
- 24355FG2
- 25148FG2
- 24325FG2
- 25029FG2
- 25069FG2
- 25085FG2
- 25216FG2
- 25274FG2
- 24348FG2
- 24354FG2
- 25055FG2
- 25014FG2
- 25161FG2
- 25101FG2
- 24353FG2
- UDI-DI
- 10197106760901
- 50197106760909
- 10197106809969
- 50197106809967
- 10198956053328
- 50198956053326
- 10198956066847
- 50198956066845
- Lot
- 24317FG2
- 24347FG2
- 24355FG2
- 25069FG2
- 25014FG2
- 25029FG2
- 24309FG2
- 24325FG2
- 24353FG2
- 25045FG2
- 25065FG2
- 25062FG2
- 25085FG2
- 25097FG2
- 25101FG2
- 25148FG2
- 25217FG2
- 24299FG2
- 25154FG2
Details
- Company began the recall
- Sold in
US Nationwide distribution in the states of California, Illinois, Kentucky, Missouri, North Carolina, New York, Ohio, Texas.
- Event ID
- 99768
- Recall numbers
- Z-3295-2026 to Z-3298-2026
- Company
- Cardinal Health 200, LLCWaukegan, Illinois
- Hazard
- Device defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
Summary updated
In FDA's weekly enforcement report
