Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001967) due to potential low dead space issues. Affected units may cause inaccurate dosing in 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 include 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 can cause medication to not fully enter the syringe, potentially leading to inaccurate dosing. This is a risk during medical procedures where precise medication amounts are critical.
Healthcare professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes may experience inaccurate dosing.
Check for the part number 58001967 on the syringe packaging. The product was sold with the UDI-DI 30886158033715 and lot number 6074600.
Look for the part number 58001967 on the syringe packaging to confirm if the product is affected.
The recall is due to low dead space syringes that could lead to inaccurate medication dosing during medical procedures.
The official notice does not specify a remedy or action steps for affected products.
The recall addresses a potential risk of inaccurate dosing, but the official notice does not mention serious injury or death.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2929-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2929-2024 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.
