Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001484) 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. These syringes have a low dead space design that could cause air embolism if used improperly.
Low dead space syringes can allow air to enter the bloodstream during injections, potentially causing air embolism. This risk is higher when syringes are used for procedures where air can be forced into the bloodstream.
Users of CustomEyes Procedure Packs with Sol-M syringes (Part Number 58001484) are affected. Healthcare professionals using these syringes for injections are most at risk.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes. The Part Number is 58001484, and Lot/Batch Numbers include 6061631 or 6062125.
Look for Part Number 58001484 on the syringe packaging or label.
The recall is for low dead space syringes that could cause air embolism if used improperly during injections.
Check for Part Number 58001484 on the syringe packaging or label, and Lot/Batch Numbers 6061631 or 6062125.
The official recall notice does not specify a remedy or action steps for affected products.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2874-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2874-2024 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.
