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RecallWatchMedical Device Safety
Class IIOngoingZ-3295-2026

Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT

Cardinal Health 200, LLCWaukegan, IL, United StatesReported Oct 7, 2026 · 6 days ago
Legal News Analyst ·

Reason for recall

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.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2) KIT, LAP CHOLE , Catalog Number: PGCGLCBAD; 3) KIT, LAP CHOLE , Catalog Number: PGCGLCBAE; 4) KIT, LAP CHOLE , Catalog Number: PGCGLCB11; 5) KIT, CARDIO MINIMALLY INVASIVE, Catalog Number: PV63CMST5; 6) HMC ROBOTIC PACK , Catalog Number: SBA23RBHNG; 7) HMC ROBOTIC PACK , Catalog Number: SBA23RBHNH; 8) ENS ENDOCHOLEYCYSTECTOMIE 4 , Catalog Number: SBA30EDCLB; 9) LAP CHOLE PACK , Catalog Number: SLC37LCJOB; 10) LAP CHOLE PACK , Catalog Number: SLC37LCJ21; 11) LAP CHOLE PACK , Catalog Number: SLC37LCJ22; 12) PACK GYNE ROBOTIC , Catalog Number: SMA30RBHSA

Lot / code information

UDI
10197106751749(each), 50197106751747(case)
Lot #
24309FG2 ; 2) PGCGLCBAC
UDI
10197106751749(each), 50197106751747(case)
Lot #
24352FG2 ; 3) PGCGLCBAC
UDI
10197106751749(each), 50197106751747(case)
Lot #
24317FG2 ; 4) PGCGLCBAC
UDI
10197106751749(each), 50197106751747(case)
Lot #
25062FG2 ; 5) PGCGLCBAD
UDI
10198956230309(each), 50198956230307(case)
Lot #
25121FG2 ; 6) PGCGLCBAD
Show 104 more code fields
UDI
10198956230309(each), 50198956230307(case)
Lot #
25045FG2 ; 7) PGCGLCBAE
UDI
10198956363366(each), 50198956363364(case)
Lot #
25217FG2 ; 8) PGCGLCB11
UDI
10198956116177(each), 50198956116175(case)
Lot #
24355FG2 ; 9) PV63CMST5
UDI
10198956526204(each), 50198956526202(case)
Lot #
25148FG2 ; 10) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
24317FG2 ; 11) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
24325FG2 ; 12) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
24317FG2 ; 13) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
25029FG2 ; 14) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
25069FG2 ; 15) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
25045FG2 ; 16) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
25069FG2 ; 17) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
24317FG2 ; 18) SBA23RBHNG
UDI
10197106417577(each), 50197106417575(case)
Lot #
25085FG2 ; 19) SBA23RBHNH
UDI
10198956332010(each), 50198956332018(case)
Lot #
25217FG2 ; 20) SBA30EDCLB
UDI
10198956286955(each), 50198956286953(case)
Lot #
25217FG2 ; 21) SBA30EDCLB
UDI
10198956286955(each), 50198956286953(case)
Lot #
25216FG2 ; 22) SBA30EDCLB
UDI
10198956286955(each), 50198956286953(case)
Lot #
25274FG2 ; 23) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24325FG2 ; 24) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24309FG2 ; 25) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24317FG2 ; 26) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24348FG2 ; 27) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24317FG2 ; 28) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24317FG2 ; 29) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24354FG2 ; 30) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24354FG2 ; 31) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25029FG2 ; 32) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25029FG2 ; 33) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25055FG2 ; 34) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24317FG2 ; 35) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25014FG2 ; 36) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25029FG2 ; 37) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25045FG2 ; 38) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25045FG2 ; 39) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25045FG2 ; 40) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25148FG2 ; 41) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25045FG2 ; 42) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25055FG2 ; 43) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25069FG2 ; 44) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25148FG2 ; 45) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25161FG2 ; 46) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25045FG2 ; 47) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25101FG2 ; 48) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25121FG2 ; 49) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25148FG2 ; 50) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
24353FG2 ; 51) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25014FG2 ; 52) SLC37LCJOB
UDI
10887488326269(each), 50887488326267(case)
Lot #
25045FG2 ; 53) SLC37LCJ21
UDI
10198956035850(each), 50198956035858(case)
Lot #
24317FG2 ; 54) SLC37LCJ22
UDI
10198956109094(each), 50198956109092(case)
Lot #
24317FG2 ; 55) SLC37LCJ22
UDI
10198956109094(each), 50198956109092(case)
Lot #
24348FG2 ; 56) SLC37LCJ22
UDI
10198956109094(each), 50198956109092(case)
Lot #
24353FG2 ; 57) SMA30RBHSA
UDI
10198956437067(each), 50198956437065(case)
Lot #
25274FG2

What the firm is doing

An URGENT: PRODUCT CORRECTION notification letter dated 8/18/26 was sent to customers. Presource has completed its investigation regarding this recall and determined that you may have received Presource kits containing the affected Stryker component(s) and lot number(s). Please reference the attached report identifying your facility s kits, along with the corresponding lot numbers that are affected by this action. If you locate affected product within your facility, please do the following: 1. QUARANTINE affected kits. 2. ALERT your clinicians of this action. 3. AFFIX a WARNING LABEL to the front of each Presource kit so that it is clearly visible to clinicians, instructing them to remove and discard the recalled component(s). 4. RETURN a copy of the enclosed Acknowledgment Form confirming your receipt of this action and the completion of labeling product via fax to 614.652.9648. Additional labels will be sent to your facility upon request. Please send an email to: gmb-FieldCorrectiveAction@cardinalhealth.com Your response to this recall notice is required Please fax this form to 614-652-9648 or email to GMB-fieldcorrectiveaction@cardinalhealth.com to acknowledge your receipt of the recall. Please respond even if you do not have recalled product on hand.

DistributionShow details

US Nationwide distribution in the states of CA, IL, KY, MO, NC, NY, OH, TX.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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