FDAClass II · Medical device · Recall Z-3296-2026 · Recalled October 7, 2026
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets recall — Cardinal Health 200, LLC
Agency report date: October 7, 2026.
1. Compare your item
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Product named
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets
Company / brand
Cardinal Health 200
Lot / serial / date codes
1) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case), Lot Number: 24317FG2 ; 2) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case), Lot Number: 24353FG2 ; 3) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case), Lot Number: 24317FG2 ; 4) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case), Lot Number: 25069FG2 ; 5) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case), Lot Number: 25045FG2 ; 6) PGVMDVBWU, UDI-DI: 10888439626186(each), 50888439626184(case), Lot Number: 25069FG2 ; 7) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case), Lot Number: 24353FG2 ; 8) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case), Lot Number: 25101FG2 ; 9) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case), Lot Number: 25148FG2 ; 10) PGVMDVBWV, UDI-DI: 10198956204034(each), 50198956204032(case), Lot Number: 25217FG2 ; 11) PGVMDVB26, UDI-DI: 10198956007796(each), 50198956007794(case), Lot Number: 24309FG2 ; 12) PGVMDVB27, UDI-DI: 10198956054714(each), 50198956054712(case), Lot Number: 24325FG2 ; 13) PGVMDVB28, UDI-DI: 10198956079847(each), 50198956079845(case), Lot Number: 24317FG2 ; 14) PGVMDVB28, UDI-DI: 10198956079847(each), 50198956079845(case), Lot Number: 24325FG2 ; 15) PGVMDVB29, UDI-DI: 10198956094024(each), 50198956094022(case), Lot Number: 24317FG2 ; 16) PGVMDVB29, UDI-DI: 10198956094024(each), 50198956094022(case), Lot Number: 24348FG2 ; 17) SBA73CLKFD, UDI-DI: 10197106633960(each), 50197106633968(case), Lot Number: 25055FG2 ; 18) SBA73CLK26, UDI-DI: 10198956029828(each), 50198956029826(case), Lot Number: 24309FG2
Distribution
US Nationwide distribution in the states of CA, IL, KY, MO, NC, NY, OH, TX.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
2. Agency hazard and consumer action
FDA reports: 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.
No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.
Class II: may cause temporary or medically reversible health consequences.
Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes;
the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.