Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001713) due to potential contamination risks.
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. This recall is due to a potential contamination risk from the syringes, which could affect medical procedures.
The syringes were manufactured by Sol-Millennium Medical (Sol-M) and may contain contaminants that could lead to infections during medical procedures. The recall is for low dead space syringes and luer slip tip syringes that were present in some CustomEyes Procedure Packs.
Medical professionals who use these syringes in procedures may be affected. Patients receiving treatments with these syringes could be at risk of contamination.
Check for the Part Number 58001713 on the syringe packaging. The product was sold with UDI-DI: 30886158032428 and Lot/Batch Number 6074823.
Look for Part Number 58001713 on the syringe packaging or check the UDI-DI: 30886158032428 and Lot/Batch Number 6074823.
The recall is due to potential contamination risks from the syringes manufactured by Sol-Millennium Medical (Sol-M).
Check the product details for the Part Number 58001713, UDI-DI: 30886158032428, and Lot/Batch Number 6074823. If you have these details, contact the manufacturer for further instructions.
The recall is for low dead space syringes and luer slip tip syringes that may contain contaminants, but the risk is considered low.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2907-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2907-2024 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.
