Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001622) due to potential air embolism risk from low dead space syringes.
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure Packs.
Beaver Visitec is recalling CustomEyes Procedure Packs that contain Sol-M Luer Lock and Luer Slip 1ml syringes (Part Number 58001622) because these syringes have a low dead space design that could cause air embolism if used improperly. This recall is important because air embolism can be serious and may require immediate medical attention.
These syringes have a low dead space design that could allow air to enter the bloodstream during injection, potentially causing air embolism. Air embolism is a serious condition where air bubbles block blood flow and can lead to complications like stroke or organ damage.
Users of CustomEyes Procedure Packs containing Sol-M syringes with Part Number 58001622 are affected. Healthcare professionals and patients using these syringes for medical procedures are most at risk.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes. The Part Number is 58001622, and the Lot/Batch Numbers are 6062867 or 6072189.
Identify if your CustomEyes Procedure Pack contains Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001622.
The Part Number is 58001622.
Lot/Batch Numbers 6062867 and 6072189 are affected.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes and Part Number 58001622.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2891-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2891-2024 from Beaver Visitec. 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.
