Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000813) due to potential low dead space causing inaccurate dosing. Affected units sold with specific batch 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 inaccurate medication dosing if the user does not properly expel air before injecting. This could lead to under-dosing of medications.
Medical professionals using CustomEyes Procedure Packs with specific batch numbers of syringes are most at risk. Patients receiving injections with these syringes may experience inaccurate dosing.
Check for CustomEyes Procedure Packs with Part Number 58000813. Affected units include batch numbers 6068010 and 6075202.
Look for batch numbers 6068010 or 6075202 on the syringe packaging.
The recall states these syringes have a low dead space design that could cause inaccurate dosing, but the official notice does not specify if they are safe to use without the recall.
The official recall notice does not provide specific action steps for users beyond checking batch numbers.
Check for batch numbers 6068010 or 6075202 on the syringe packaging.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2827-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2827-2024 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.
