Medline medical procedure convenience kits labeled as recallZ-1087-2026 · Medline Industries, LP · initiated Dec 16, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
FDA root cause category: Under Investigation by firm
What the company is doing
Medline Industries issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 12/16/2025 via email and USPS first class mail. The notice explained the issue, potential risk, and requested the following: "1.Immediately check your stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. 2.Please use the link and the information below to complete your response form. Please list the quantityof affected product you have in inventory on the form. Even if you do not have any affected productin inventory, please complete and submit the form. Website link: https://recalls.medline.comRecall Reference #: R-25-145-FGX5 Recall Code: 3.Upon receipt of your submitted response form, your account will receive over-labels to place on affected inventory, with instructions for your staff to remove and discard the affected component prior to using the kit. These labels will be provided via FedEx overnight, if applicable. 4.If you are a distributor or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please include your customers quantities on your response form. Upon receipt of your submitted response form, you will receive over-labels to provide to your customers to affix to their affected product. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected]."
Recall details
- Recall number
- Z-1087-2026
- Status
- Open, Classified
- Initiated by the company
- Dec 16, 2025
- Posted by the FDA
- Jan 14, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 4536 units
- Product code
- LRO
- Distribution
- US Nationwide distribution.
Product description
Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHOLE PACK, REF DYNJ57640F; 7) GYN/PROSTATE ROBOTIC PACK, REF DYNJ62594D; 8) RR-DAVINCI PROSTATE ACCESSORY, REF DYNJ63392D; 9) LAPAROSCOPY PACK, REF DYNJ68187B; 10) LAPAROSCOPY PACK, REF DYNJ82368A; 11) ROBOTIC KIDNEY PACK, REF DYNJ85261; 12) DOWNTOWN ROBOTICS, REF DYNJ86178B; 13) DAVINCI LITHOTOMY PACK, REF DYNJ87610; 14) ROBOTIC WHIPPLE PACK, REF DYNJ88433; 15) PROSTATE DAVINCI, REF DYNJ900127G; 16) GENERAL LAPAROSCOPY, REF DYNJ901847M; 17) LAG TLH, REF DYNJ901890N; 18) LITHOTOMY ROBOTIC CDS, REF DYNJ903948S; 19) LAP, REF DYNJ904576B; 20) ROBOTIC, REF DYNJ905147B; 21) ROBOTICS GYN, REF DYNJ905824M; 22) WH DAVINCI TLH PROCEDURE, REF DYNJ905920B; 23) CHN OR BASIC ROBOTIC, REF DYNJ905982I; 24) KIT ROBOTIC RFD, REF DYNJ906311F; 25) ROBOTIC PROSTATE, REF DYNJ906381G; 26) DAVINCI, REF DYNJ907392C; 27) CHIASSON GASTRIC SLEEVE KIT, REF DYNJ907405C; 28) GYN, REF DYNJ908504B; 29) UROLOGY ROBOTIC, REF DYNJ908588I; 30) THORACIC ROBOTICS, REF DYNJ908777A; 31) GENERAL ROBOT, REF DYNJ908969A; 32) KIT ROBOTIC, REF DYNJ909870B; 33) ROBOTIC THORACOSCOPY, REF DYNJ910924.
Code information (models, lots, serial numbers)
Show the full code information (6k characters)
REF CDS860237AF: UDI/DI 10198459232626 (EA) 40198459232627 (CS), Lot Number 25FBK870; REF CDS860237AF: UDI/DI 10198459232626 (EA) 40198459232627 (CS), Lot Number 25EBD110; REF CDS982128Q: UDI/DI 10198459008245 (EA) 40198459008246 (CS), Lot Number 25EBC253; REF CDS982128Q: UDI/DI 10198459008245 (EA) 40198459008246 (CS), Lot Number 25DBG393; REF CDS984338M: UDI/DI 10198459148101 (EA) 40198459148102 (CS), Lot Number 25FBQ303; REF CDS984338M: UDI/DI 10198459148101 (EA) 40198459148102 (CS), Lot Number 25EBD631; REF CDS984338M: UDI/DI 10198459148101 (EA) 40198459148102 (CS), Lot Number 25DBM322; REF CDS984640I: UDI/DI 10198459318955 (EA) 40198459318956 (CS), Lot Number 25DBT807; REF DYNJ0525321O: UDI/DI 10198459236907 (EA) 40198459236908 (CS), Lot Number 25DMG099; REF DYNJ0525321O: UDI/DI 10198459236907 (EA) 40198459236908 (CS), Lot Number 25CMJ006; REF DYNJ57640F: UDI/DI 10198459011115 (EA) 40198459011116 (CS), Lot Number 25FDB347; REF DYNJ62594D: UDI/DI 10198459049767 (EA) 40198459049768 (CS), Lot Number 25EBK539; REF DYNJ62594D: UDI/DI 10198459049767 (EA) 40198459049768 (CS), Lot Number 25DBD145; REF DYNJ63392D: UDI/DI 10198459164507 (EA) 40198459164508 (CS), Lot Number 25BLA967; REF DYNJ68187B: UDI/DI 10198459382086 (EA) 40198459382087 (CS), Lot Number 25FMG440; REF DYNJ82368A: UDI/DI 10198459258077 (EA) 40198459258078 (CS), Lot Number 25EMH020; REF DYNJ82368A: UDI/DI 10198459258077 (EA) 40198459258078 (CS), Lot Number 25CMF917; REF DYNJ85261: UDI/DI 10195327483418 (EA) 40195327483419 (CS), Lot Number 25FBK331; REF DYNJ85261: UDI/DI 10195327483418 (EA) 40195327483419 (CS), Lot Number 25EBR783; REF DYNJ86178B: UDI/DI 10198459104800 (EA) 40198459104801 (CS), Lot Number 25EBP320; REF DYNJ86178B: UDI/DI 10198459104800 (EA) 40198459104801 (CS), Lot Number 25EBC981; REF DYNJ86178B: UDI/DI 10198459104800 (EA) 40198459104801 (CS), Lot Number 25DBA834; REF DYNJ86178B: UDI/DI 10198459104800 (EA) 40198459104801 (CS), Lot Number 25CBM884; REF DYNJ87610: UDI/DI 10198459047817 (EA) 40198459047818 (CS), Lot Number 25FBK123; REF DYNJ87610: UDI/DI 10198459047817 (EA) 40198459047818 (CS), Lot Number 25EBF929; REF DYNJ87610: UDI/DI 10198459047817 (EA) 40198459047818 (CS), Lot Number 25CBT135; REF DYNJ88433: UDI/DI 10198459157936 (EA) 40198459157937 (CS), Lot Number 25FMC215; REF DYNJ88433: UDI/DI 10198459157936 (EA) 40198459157937 (CS), Lot Number 25EMF199; REF DYNJ88433: UDI/DI 10198459157936 (EA) 40198459157937 (CS), Lot Number 25EMC621; REF DYNJ900127G: UDI/DI 10193489851588 (EA) 40193489851589 (CS), Lot Number 25FBO994; REF DYNJ900127G: UDI/DI 10193489851588 (EA) 40193489851589 (CS), Lot Number 25EBE439; REF DYNJ901847M: UDI/DI 10198459037863 (EA) 40198459037864 (CS), Lot Number 25BBM364; REF DYNJ901890N: UDI/DI 10198459300592 (EA) 40198459300593 (CS), Lot Number 25FBJ408; REF DYNJ901890N: UDI/DI 10198459300592 (EA) 40198459300593 (CS), Lot Number 25EBJ877; REF DYNJ903948S: UDI/DI 10198459332883 (EA) 40198459332884 (CS), Lot Number 25EBO236; REF DYNJ903948S: UDI/DI 10198459332883 (EA) 40198459332884 (CS), Lot Number 25EBC133; REF DYNJ904576B: UDI/DI 10888277776760 (EA) 40888277776761 (CS), Lot Number 25DMH506; REF DYNJ904576B: UDI/DI 10888277776760 (EA) 40888277776761 (CS), Lot Number 25DMD329; REF DYNJ905147B: UDI/DI 10193489569032 (EA) 40193489569033 (CS), Lot Number 25GDB060; REF DYNJ905824M: UDI/DI 10198459303272 (EA) 40198459303273 (CS), Lot Number 25DMK337; REF DYNJ905824M: UDI/DI 10198459303272 (EA) 40198459303273 (CS), Lot Number 25CMF465; REF DYNJ905920B: UDI/DI 10195327592707 (EA) 40195327592708 (CS), Lot Number 25EBG945; REF DYNJ905920B: UDI/DI 10195327592707 (EA) 40195327592708 (CS), Lot Number 25CBM218; REF DYNJ905982I: UDI/DI 10195327251420 (EA) 40195327251421 (CS), Lot Number 25EMD118; REF DYNJ905982I: UDI/DI 10195327251420 (EA) 40195327251421 (CS), Lot Number 25DMJ823; REF DYNJ905982I: UDI/DI 10195327251420 (EA) 40195327251421 (CS), Lot Number 25CMJ265; REF DYNJ905982I: UDI/DI 10195327251420 (EA) 40195327251421 (CS), Lot Number 25CMC374; REF DYNJ905982I: UDI/DI 10195327251420 (EA) 40195327251421 (CS), Lot Number 25CMC546; REF DYNJ906311F: UDI/DI 10198459080494 (EA) 40198459080495 (CS), Lot Number 25EBI860; REF DYNJ906311F: UDI/DI 10198459080494 (EA) 40198459080495 (CS), Lot Number 25DBR934; REF DYNJ906311F: UDI/DI 10198459080494 (EA) 40198459080495 (CS), Lot Number 25CBF096; REF DYNJ906381G: UDI/DI 10198459131066 (EA) 40198459131067 (CS), Lot Number 25FBJ655; REF DYNJ906381G: UDI/DI 10198459131066 (EA) 40198459131067 (CS), Lot Number 25FBE873; REF DYNJ906381G: UDI/DI 10198459131066 (EA) 40198459131067 (CS), Lot Number 25EBB258; REF DYNJ906381G: UDI/DI 10198459131066 (EA) 40198459131067 (CS), Lot Number 25DBR935; REF DYNJ907392C: UDI/DI 10195327541378 (EA) 40195327541379 (CS), Lot Number 25DMH137; REF DYNJ907392C: UDI/DI 10195327541378 (EA) 40195327541379 (CS), Lot Number 25CMJ730; REF DYNJ907405C: UDI/DI 10195327541392 (EA) 40195327541393 (CS), Lot Number 25CMF429; REF DYNJ908504B: UDI/DI 10198459318221 (EA) 40198459318222 (CS), Lot Number 25FBG752; REF DYNJ908504B: UDI/DI 10198459318221 (EA) 40198459318222 (CS), Lot Number 25DBS537; REF DYNJ908588I: UDI/DI 10198459231544 (EA) 40198459231545 (CS), Lot Number 25FDA930; REF DYNJ908588I: UDI/DI 10198459231544 (EA) 40198459231545 (CS), Lot Number 25EDB953; REF DYNJ908588I: UDI/DI 10198459231544 (EA) 40198459231545 (CS), Lot Number 25EDA576; REF DYNJ908588I: UDI/DI 10198459231544 (EA) 40198459231545 (CS), Lot Number 25DDA437; REF DYNJ908588I: UDI/DI 10198459231544 (EA) 40198459231545 (CS), Lot Number 25CDB060; REF DYNJ908777A: UDI/DI 10195327415174 (EA) 40195327415175 (CS), Lot Number 25CBA577; REF DYNJ908777A: UDI/DI 10195327415174 (EA) 40195327415175 (CS), Lot Number 25CBA577Z; REF DYNJ908969A: UDI/DI 10198459003950 (EA) 40198459003951 (CS), Lot Number 25EBI127; REF DYNJ908969A: UDI/DI 10198459003950 (EA) 40198459003951 (CS), Lot Number 25CBP413; REF DYNJ908969A: UDI/DI 10198459003950 (EA) 40198459003951 (CS), Lot Number 25CBD522; REF DYNJ909870B: UDI/DI 10198459122446 (EA) 40198459122447 (CS), Lot Number 25EBF813; REF DYNJ909870B: UDI/DI 10198459122446 (EA) 40198459122447 (CS), Lot Number 25DBD407; REF DYNJ910924: UDI/DI 10198459203442 (EA) 40198459203443 (CS), Lot Number 25EBK656.
Devices named in this recall
30 devices in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJ907405CMedline Industries, Inc. · General surgery tray3 recalls0 reports
- Medline Industries, Inc. DYNJ82368AMedline Industries, Inc. · General surgery tray3 recalls0 reports
- Medline Industries, Inc. DYNJ904576BMedline Industries, Inc. · General surgery tray3 recalls0 reports
- Medline Industries, Inc. DYNJ908777AMedline Industries, Inc. · Cardiovascular procedure kit2 recalls0 reports
- Medline Industries, Inc. DYNJ85261Medline Industries, Inc. · General surgery tray2 recalls0 reports
- Medline Industries, Inc. DYNJ907392CMedline Industries, Inc. · General surgery tray2 recalls0 reports
- Medline Industries, Inc. DYNJ905147BMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ900127GMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ905982IMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ905920BMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ908969AMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. CDS982128QMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ57640FMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ901847MMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ87610Medline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ62594DMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ906311FMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ86178BMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ909870BMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ906381GMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. CDS984338MMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ88433Medline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ63392DMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ910924Medline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ908588IMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. CDS860237AFMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ0525321OMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. DYNJ908504BMedline Industries, Inc. · General surgery tray1 recall0 reports
- Medline Industries, Inc. CDS984640IMedline Industries, Inc. · General surgery tray1 recall0 reports
- MEDLINE INDUSTRIES, INC. DYNJ68187BMedline Industries, Inc. · General surgery tray1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 98197).
- Z-1085-2026 · Open, ClassifiedMedline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
- Z-1086-2026 · Open, ClassifiedMedline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF, REF CDS860235L; 2) GENERAL LAPAROSCOPIC, REF CDS930223M; 3) LAP CHOLE CDS, REF CDS983678K; 4) LAP…
- Z-1088-2026 · Open, ClassifiedMedline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-…
- Z-1089-2026 · Open, ClassifiedMedline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE, REF CDS980754T; 2) GYN LAP HYSTERECTOMY CDS, REF CDS982662Q; 3) DAVINCI HYSTERECTOMY CDS, REF CDS98534…
- Z-1090-2026 · Open, ClassifiedMedline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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