Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001073) due to potential low dead space causing inaccurate dosing. 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. These syringes have a low dead space design that could lead to inaccurate medication dosing if used improperly.
The syringes have a low dead space design that can cause medication to be delivered in smaller volumes than intended. This may lead to inaccurate dosing if the syringe is not properly filled or used.
Medical professionals using CustomEyes Procedure Packs for injections or procedures are most at risk. Patients receiving treatments with these syringes may experience inaccurate dosing.
Check for the Part Number 58001073 on the syringe packaging. The lot number 6070760 and UDI-DI 30886158021934 are also associated with this recall.
Look for the Part Number 58001073 on the syringe packaging to identify affected units.
The recall states these syringes have a low dead space design that could lead to inaccurate dosing, but no specific safety warnings are provided.
Check for the Part Number 58001073 on the syringe packaging. The lot number 6070760 and UDI-DI 30886158021934 are also associated with this recall.
The recall does not specify a remedy or action steps for affected users.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2842-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2842-2024 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.
