Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001304) due to potential low dead space issues. Affected units may cause inaccurate dosing if used improperly.
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 dosing if used incorrectly, potentially causing medication errors.
The syringes have a low dead space design that may not properly hold medication, leading to inaccurate dosing when used. This could cause medication errors if the syringe is not properly filled or if air is trapped in the syringe.
Medical professionals using CustomEyes Procedure Packs with the specific syringes (Part Number 58001304) are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing.
Check for the Part Number 58001304 on the syringe packaging. The affected packs also have UDI-DI: 30886158023778 and Lot/Batch Number 6069386.
Look for Part Number 58001304 on the syringe packaging or the CustomEyes Procedure Pack label.
The specific part number is 58001304.
Check for Part Number 58001304 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall does not specify a remedy, so you should check with the manufacturer or healthcare provider for guidance.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2854-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2854-2024 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.
