Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001795) 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 (part number 58001795) because these syringes have a low dead space that could lead to inaccurate medication dosing. This recall affects healthcare professionals using these syringes for procedures where precise dosing is critical.
The syringes have a low dead space, meaning small amounts of liquid can remain in the syringe after drawing medication. This could cause inaccurate dosing if the liquid is not fully expelled before administration, potentially leading to underdosing.
Healthcare professionals who use CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing if the syringes are used improperly.
Check for the part number 58001795 on the syringe packaging. The product was sold with specific lot/batch numbers and UDI-DI codes listed in the recall notice.
Look for part number 58001795 on the syringe packaging to confirm if the product is affected.
The part number is 58001795.
Check for part number 58001795 on the syringe packaging. The product was sold with specific lot/batch numbers and UDI-DI codes listed in the recall notice.
The recall does not mention a fix; affected products should be checked and discarded if they have the part number 58001795.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2914-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2914-2024 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.
