Medline recalls two medical procedure kits with Strykeflow 2 Suction Irrigators that may leak saline vapor during use, posing a risk of confusion with smoke. Affected kits have specific model 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 medical procedure kits that include Strykeflow 2 Suction Irrigators. These kits may leak saline vapor that can resemble smoke, potentially causing confusion during medical procedures.
The design change in 2024 allows irrigation solution to travel to the handpiece and battery pack. This can cause leaks or vaporized saline that looks like smoke during use, which might be mistaken for actual smoke.
Medical professionals using the recalled kits are most at risk. The recall affects specific models sold in 2024 with particular lot numbers.
Check for kits labeled 'THORACIC ROBOTICS, REF DYNJ908777B' or 'CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359'. The lot numbers 25EBD732 or 25FBA103 indicate affected units.
Look for specific model labels and lot numbers on the kits to confirm if they are affected.
The recall is due to a design change in 2024 that causes irrigation solution to leak or emit vaporized saline during use, which can resemble smoke.
The official notice does not specify a remedy, so check with Medline directly for further instructions.
Affected kits have model labels like 'THORACIC ROBOTICS, REF DYNJ908777B' or 'CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359' with lot numbers 25EBD732 or 25FBA103.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1085-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1085-2026 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.
