Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001943) due to potential low dead space causing inaccurate dosing. Affected users should check product details.
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 58001943) because these syringes have a low dead space that could lead to inaccurate dosing during medical procedures. This recall matters because improper dosing could affect treatment outcomes.
The syringes have a low dead space, meaning small amounts of liquid can remain in the syringe after drawing. This could cause inaccurate dosing if the liquid is not fully expelled before use, potentially affecting treatment effectiveness.
Healthcare professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes may also be affected.
Check for the part number 58001943 on the syringe packaging. The product was sold with UDI-DI: 30886158033623 and lot number 6071510.
Look for part number 58001943 on the syringe packaging or the product label.
The part number is 58001943.
Check for part number 58001943 on the syringe packaging or the product label.
The recall does not provide a fix; the remedy is not stated in the record.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2927-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2927-2024 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.
