Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001928) due to potential low dead space causing inaccurate dosing.
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 lead to inaccurate medication dosing if used improperly.
The syringes have a low dead space design that can cause medication to be delivered in smaller volumes than intended. This may lead to inaccurate dosing if the syringes are not used properly during medical procedures.
Medical professionals using CustomEyes Procedure Packs with the specific syringe part numbers are affected. Patients receiving treatments with these syringes may face inaccurate dosing if the syringes are used incorrectly.
Check for the part number 58001928 on the syringe packaging. The product was sold with UDI-DI: 30886158033777 and lot number 6074346.
Look for part number 58001928 on the syringe packaging to identify affected units.
The recall is due to low dead space syringes that could cause inaccurate medication dosing if used improperly.
Check the syringe packaging for part number 58001928 to determine if they are affected. If so, stop using them and contact Beaver Visitec for further instructions.
The low dead space design may lead to inaccurate dosing, but the recall is for low risk as the hazard is not severe in normal use.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2924-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2924-2024 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.
