Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001417) due to potential low dead space causing inaccurate dosing. Affected units sold with specific lot 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 have a low dead space that could lead to inaccurate dosing during medical procedures.
The syringes have a low dead space, meaning small amounts of fluid can remain in the syringe after use. This could cause inaccurate dosing of medications or fluids during medical procedures, potentially leading to underdosing.
Medical professionals using CustomEyes Procedure Packs with the specific syringe part numbers are most at risk. Patients receiving these syringes during procedures may also be affected.
Check for the part number 58001417 on the syringe packaging. Affected packs were sold with lot numbers 6071011 or 6072526.
Look for part number 58001417 on the syringe packaging or label.
The recall is due to low dead space syringes that could cause inaccurate dosing during medical procedures.
Part number 58001417 for Sol-M Luer Lock and Luer Slip 1ml syringes.
Check for lot numbers 6071011 or 6072526 on the packaging.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2870-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2870-2024 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.