Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001376) due to potential contamination risks. Affected units sold with specific batch numbers.
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 may have a risk of contamination if used improperly, which could lead to health issues.
The syringes were manufactured by Sol-M and may contain contaminants due to a low dead space design. This could lead to infections or other health issues if the syringes are used without proper cleaning.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures with these syringes could also be affected.
Check for the Part Number 58001376 on the syringe packaging. Affected packs were sold with batch numbers 6062023 or 6064080.
Look for the Part Number 58001376 on the syringe packaging or the CustomEyes Procedure Pack label.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001376.
Affected packs have batch numbers 6062023 or 6064080.
The recall does not specify a stop-use action, so you can continue using them if they are not contaminated.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2864-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2864-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
