Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001629) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part 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 not fully enter the syringe, leading to inaccurate dosing. This could result in under-dosing medications if the syringe is not properly filled.
Healthcare professionals using CustomEyes Procedure Packs for medical injections are most at risk. Patients receiving injections with these syringes may experience inaccurate dosing.
Check for the part number 58001629 on the syringe packaging. The product was sold with specific lot numbers including 6061298.
Look for the part number 58001629 on the syringe packaging to identify affected units.
The recall is due to low dead space syringes that could cause inaccurate medication dosing if used improperly.
Part number 58001629 is the affected syringe model.
Check for the part number 58001629 on the syringe packaging or look for lot number 6061298.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2893-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2893-2024 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.
