Medline is recalling 73 medical convenience kits labeled with specific model numbers and lot numbers due to potential issues with SafeAir Smoke Evacuation Pencil components.
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
Medline is recalling 73 different medical convenience kits used in gynecology and robotic procedures. These kits were manufactured using certain lots of SafeAir Smoke Evacuation Pencil that were previously recalled by Stryker. The recall is because these kits may contain defective components that could pose a safety risk.
The recall is linked to SafeAir Smoke Evacuation Pencil components that were previously recalled by Stryker. While the exact hazard isn't specified in the notice, the fact that these components were previously recalled suggests potential safety issues.
Medical professionals who use these kits during surgeries or procedures are likely affected. The risk is highest for those handling the recalled kits without proper checks.
Check for kits labeled with model numbers like CDS760059I, CDS920099S, or DYNJ series codes. The specific lot numbers listed in the recall record (e.g., 22KBT168, 22GBJ110) indicate which kits are affected.
Look for model numbers and lot numbers listed in the recall record to determine if your kit is affected.
Medline is recalling these kits because they were manufactured using certain lots of SafeAir Smoke Evacuation Pencil that were previously recalled by Stryker.
Check the model number and lot number on your kit against the list provided in the recall record.
The recall notice does not specify a remedy, so you should check with Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0643-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0643-2025 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.