Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000921) 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 Sol-M Luer Lock and Luer Slip 1ml syringes. 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, meaning small amounts of fluid can remain in the syringe after drawing medication. If the syringe is not properly cleared of this residual fluid before use, it could lead to inaccurate dosing of medication.
Medical professionals using CustomEyes Procedure Packs with the specific syringes 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 58000921 on the syringes. The product was sold with UDI-DI: 30886158021309 and Lot/Batch Number 6073120.
Look for the Part Number 58000921 on the syringes to confirm if they are affected.
The recall states these syringes have a low dead space design that could lead to inaccurate dosing if not properly cleared of residual fluid. They are not safe for use without proper verification.
The recall does not specify a remedy, so check the syringe details to confirm if they are affected. If affected, contact the manufacturer for further instructions.
Look for the Part Number 58000921 on the syringes, or check the UDI-DI: 30886158021309 and Lot/Batch Number 6073120.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2833-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2833-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
