Medline recalls specific convenience kits containing SafeAir Smoke Evacuation Pencils from certain lots that were previously recalled by Stryker. These kits pose a risk of serious injury if used improperly.
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
Medline is recalling specific medical convenience kits that contain SafeAir Smoke Evacuation Pencils from certain lots. These products were previously recalled by Stryker due to safety concerns, and using them could lead to serious injury.
The hazard comes from SafeAir Smoke Evacuation Pencils that were manufactured using certain lots of materials previously recalled by Stryker. These pencils could cause serious injury if used incorrectly, such as during medical procedures.
Healthcare professionals and medical facilities that use these convenience kits are most at risk. The specific kits are labeled with unique identifiers and lot numbers.
Check for kits labeled with specific identifiers like ANGIO PACK #2 (REFDYNJ39185D), CV MINOR CATH LAB PACK (REFDYNJ44997J), or other listed models. Look for lot numbers such as 22GBA088, 22FBS934, or 22HBA086.
Look for the specific model numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
These kits contain SafeAir Smoke Evacuation Pencils that were previously recalled by Stryker due to safety concerns.
Check for specific model numbers and lot numbers listed in the recall notice, such as ANGIO PACK #2 (REFDYNJ39185D) or CV MINOR CATH LAB PACK (REFDYNJ44997J).
The recall notice does not specify a remedy, so contact 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-0624-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0624-2025 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.
