Medline recalls 13 types of surgical kits that contain Strykeflow 2 suction irrigators with a design change causing saline vapor leaks during use. Affected kits have specific model numbers and lot numbers.
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.
Medline is recalling 13 different surgical procedure kits that include Strykeflow 2 suction irrigators. The design change from 2024 can cause irrigation solution to leak and emit vaporized saline that resembles smoke during use.
The design change in 2024 allows irrigation solution to travel to the handpiece and battery pack during use. This can cause leaks and vaporized saline that may resemble smoke, potentially causing discomfort or respiratory issues.
Healthcare professionals using these kits during procedures are most at risk. Patients receiving surgery with these kits could be exposed to saline vapor.
Check for model numbers like CDS980754T, CDS982662Q, or DYNJ9041R on the kit. Look for specific lot numbers such as 25EMD795 or 25EBR237.
Identify the model number on the kit label to determine if it's affected.
Reach out to Medline directly for assistance with the recall.
The design change in 2024 allows irrigation solution to leak and emit vaporized saline that resembles smoke during use.
Check for model numbers like CDS980754T, CDS982662Q, or DYNJ9041R on the kit label and specific lot numbers such as 25EMD795 or 25EBR237.
Contact Medline directly for assistance with the recall.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1089-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1089-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
