Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001818) 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 specific syringes from Sol-M. These syringes have a low dead space design that could lead to inaccurate dosing if used incorrectly, which might affect medical treatments.
The syringes have a low dead space design that may not properly measure medication, leading to inaccurate dosing. This could cause underdosing or overdosing during medical procedures if the syringes are used incorrectly.
Healthcare professionals using the CustomEyes Procedure Packs for medical procedures are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing if the syringes are used improperly.
Check for the Part Number 58001818 on the syringe packaging. The product was sold with UDI-DI: 30886158033180 and Lot/Batch Number 6075189.
Verify the Part Number 58001818 on the syringe packaging to confirm if the product is affected.
The recall is due to low dead space syringes that may cause inaccurate dosing if used incorrectly during medical procedures.
The official notice does not specify a remedy or action for affected products.
Look for the Part Number 58001818 on the syringe packaging, UDI-DI: 30886158033180, and Lot/Batch Number 6075189.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2916-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2916-2024 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.
