Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001338) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers and batch codes.
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 during medical procedures, which may cause treatment errors.
The syringes have a low dead space design that may not properly hold medication, leading to inaccurate dosing during medical procedures. This could result in treatment errors if the medication dose is too low or too high.
Medical professionals using CustomEyes Procedure Packs with the specific syringe part number 58001338 are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing.
Check for the part number 58001338 on the syringe packaging. The product was sold with specific batch codes and lot numbers, including 6074329.
Look for the part number 58001338 on the syringe packaging to identify affected units.
The recall is due to low dead space syringes that could lead to inaccurate dosing during medical procedures.
Check the syringe packaging for part number 58001338 to determine if it's affected. If so, stop using it and contact the manufacturer.
The low dead space design may cause inaccurate dosing, but the recall is for low-risk correction to prevent treatment errors.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2860-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2860-2024 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.
