Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000866) due to potential low dead space issues. Affected units sold with specific lot 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 (Part Number 58000866) because these syringes have a low dead space design that could cause issues during medical procedures. This recall matters because improper use of low dead space syringes might lead to inaccurate dosing or other complications.
Low dead space syringes can cause inaccurate dosing if air is trapped in the syringe barrel during medical procedures. This may lead to under-dosing of medication or other complications depending on the procedure.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures using these syringes may also be affected.
Check for the Part Number 58000866 on the syringe packaging. Affected packs were sold with Lot/Batch Number 6074581 or UDI-DI 30886158021132.
Look for Part Number 58000866 on the syringe packaging or label.
The recall is for low dead space syringes that could cause inaccurate dosing during medical procedures.
The official notice does not specify a remedy or action for affected syringes.
Check for Part Number 58000866 on the syringe packaging or Lot/Batch Number 6074581.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2829-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2829-2024 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.
