Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000594) due to potential low dead space issues. Affected units may cause inaccurate dosing during medical procedures.
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 during medical procedures.
The syringes have a low dead space design that may cause medication to not fully mix with the solution before injection. This could lead to inaccurate dosing during medical procedures.
Medical professionals using these syringes for procedures are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing.
Check for the Part Number 58000594 on the syringe packaging. The product was sold with UDI-DI: 30886158019948 and Lot/Batch Number 6073112.
Look for the Part Number 58000594 on the syringe packaging or the UDI-DI: 30886158019948 and Lot/Batch Number 6073112.
The syringes have a low dead space design that may cause medication to not fully mix with the solution before injection, potentially leading to inaccurate dosing during medical procedures.
Check for the Part Number 58000594 on the syringe packaging or the UDI-DI: 30886158019948 and Lot/Batch Number 6073112.
The recall does not specify a stop-use action, but you should check if your syringes have the Part Number 58000594 to ensure they are safe.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2815-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2815-2024 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.
