Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT
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, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLAC; 2) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA1; 3) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA2; 4) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA3; 5) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA4; 6) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNLD; 7) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNLE; 8) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNL5; 9) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNL6; 10) MVHS GU GYN ROBOT PACK , Catalog Number: SOTDKGREFB
Lot / code information
- UDI
- 10197106760901(each), 50197106760909(case)
- Lot #
- 24317FG2 ; 2) PB23GLNLAC
- UDI
- 10197106760901(each), 50197106760909(case)
- Lot #
- 24347FG2 ; 3) PB23GLNLAC
- UDI
- 10197106760901(each), 50197106760909(case)
- Lot #
- 24355FG2 ; 4) PB23GLNLAC
- UDI
- 10197106760901(each), 50197106760909(case)
- Lot #
- 25069FG2 ; 5) PB23GLNLAC
- UDI
- 10197106760901(each), 50197106760909(case)
- Lot #
- 25014FG2 ; 6) PB23GLNLAC
- UDI
- 10197106760901(each), 50197106760909(case)
- Lot #
- 25029FG2 ; 7) PB23GLNLA1
- UDI
- 10197106809969(each), 50197106809967(case)
- Lot #
- 20 ; 8) PB23GLNLA2
- UDI
- 10198956053328(each), 50198956053326(case)
- Lot #
- 24317FG2 ; 9) PB23GLNLA3
- UDI
- 10198956066847(each), 50198956066845(case)
- Lot #
- 24309FG2 ; 10) PB23GLNLA3
- UDI
- 10198956066847(each), 50198956066845(case)
- Lot #
- 24317FG2 ; 11) PB23GLNLA3
- UDI
- 10198956066847(each), 50198956066845(case)
- Lot #
- 24325FG2 ; 12) PB23GLNLA4
- UDI
- 10198956072664(each), 50198956072662(case)
- Lot #
- 24317FG2 ; 13) PB23GLNLA4
- UDI
- 10198956072664(each), 50198956072662(case)
- Lot #
- 24325FG2 ; 14) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 24353FG2 ; 15) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 24355FG2 ; 16) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 24317FG2 ; 17) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 24353FG2 ; 18) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 24353FG2 ; 19) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25029FG2 ; 20) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25045FG2 ; 21) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 24317FG2 ; 22) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25065FG2 ; 23) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25062FG2 ; 24) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25085FG2 ; 25) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25097FG2 ; 26) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25101FG2 ; 27) PB23GRNLD
- UDI
- 10197106968963(each), 50197106968961(case)
- Lot #
- 25148FG2 ; 28) PB23GRNLE
- UDI
- 10198956320178(each), 50198956320176(case)
- Lot #
- 25217FG2 ; 29) PB23GRNL5
- UDI
- 10198956050419(each), 50198956050417(case)
- Lot #
- 24325FG2 ; 30) PB23GRNL6
- UDI
- 10198956067806(each), 50198956067804(case)
- Lot #
- 24299FG2 ; 31) PB23GRNL6
- UDI
- 10198956067806(each), 50198956067804(case)
- Lot #
- 24317FG2 ; 32) PB23GRNL6
- UDI
- 10198956067806(each), 50198956067804(case)
- Lot #
- 24325FG2 ; 33) SOTDKGREFB
- UDI
- 10198956112766(each), 50198956112764(case)
- Lot #
- 25154FG2
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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 detailsHide
US Nationwide distribution in the states of CA, IL, KY, MO, NC, NY, OH, TX.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-3297-2026
- FDA device classification · OHDOfficial FDA classification for this device type
- CFR regulation · 21 CFR 884.1720The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Cardinal Health 200, LLCSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
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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