Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000023) due to potential air embolism risk during medical procedures.
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 specific syringes from Sol-M. These syringes could cause air embolism if used incorrectly during medical procedures.
The syringes have a low dead space design that could allow air to enter the bloodstream during injections, potentially causing air embolism. This risk is higher when used in medical procedures where precise fluid delivery is critical.
Medical professionals using these syringes for procedures are most at risk. Patients receiving injections with these syringes may also be affected.
Check for the Part Number 58000023 on the syringe packaging. The product was sold with UDI-DI 30886158009253 and Lot/Batch Number 6073123.
Look for Part Number 58000023 on the syringe packaging to identify affected units.
The recall is due to potential air embolism risk from low dead space syringes used in medical procedures.
Check the syringe packaging for Part Number 58000023. If you have these syringes, contact Beaver Visitec for guidance.
These syringes could cause air embolism if used incorrectly during medical procedures, which is a low risk but requires careful handling.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2794-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2794-2024 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.
