Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001394) 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 58001394) because these syringes have a low dead space that could cause inaccurate dosing during medical procedures. This recall matters because improper dosing could lead to treatment errors.
The syringes have a low dead space, meaning small amounts of liquid may remain in the syringe after drawing. This could cause inaccurate dosing when administering medication or fluids, potentially leading to treatment errors.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes could be affected if dosing is inaccurate.
Check for the part number 58001394 on the syringe packaging. The recall includes CustomEyes Procedure Packs that contain Sol-M Luer Lock and Luer Slip 1ml syringes. These were sold with specific lot numbers and UDI-DI codes.
Look for the part number 58001394 on the syringe packaging to identify affected units.
The recall is due to low dead space syringes that could cause inaccurate dosing during medical procedures.
Check the syringe packaging for part number 58001394 to determine if they are affected. If so, contact Beaver Visitec for guidance.
The low dead space could cause inaccurate dosing, but the recall is for potential treatment errors, not immediate injury risks.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2867-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2867-2024 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.
