Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001631) 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, potentially causing medication errors.
The syringes have a low dead space design that may not properly hold medication, leading to inaccurate dosing. This could cause medication errors if the syringes are used incorrectly during procedures.
Healthcare professionals using CustomEyes Procedure Packs with the specific syringes are most at risk. Patients receiving treatments with these syringes could experience medication errors if the syringes are used improperly.
Check for the Part Number 58001631 on the syringe packaging. The product was sold with UDI-DI: 30886158031780 and Lot/Batch Number 6061721.
Look for Part Number 58001631 on the syringe packaging to confirm if the product is affected.
The Part Number is 58001631.
Check for Part Number 58001631 on the syringe packaging. The product was sold with UDI-DI: 30886158031780 and Lot/Batch Number 6061721.
The recall does not require immediate discontinuation; check the packaging to confirm if the product is affected.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2894-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2894-2024 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.
