Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001020) due to potential low dead space causing inaccurate dosing. 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 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 inaccurate medication dosing if not properly filled. This could lead to underdosing or overdosing depending on the procedure.
Healthcare professionals using these syringes for medical procedures are most at risk. Patients receiving treatments with these syringes may experience inaccurate dosing.
Check for the Part Number 58001020 on the syringe packaging. Affected packs were sold with specific batch numbers including 6068035.
Look for Part Number 58001020 on the syringe packaging or label.
The recall is due to low dead space syringes that could cause inaccurate medication dosing if not properly filled.
Check the syringe packaging for Part Number 58001020. If found, contact Beaver Visitec for guidance.
The low dead space design could lead to inaccurate dosing, but the recall is for low risk under normal use conditions.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2838-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2838-2024 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.
