Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001934) due to potential low dead space causing inaccurate dosing.
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 58001934) because these syringes have a low dead space that could lead to inaccurate medication dosing. This recall matters because improper dosing could cause harm during medical procedures.
These syringes have a low dead space, meaning small amounts of liquid may remain in the syringe after drawing medication. This can cause inaccurate dosing when transferring medication to other containers or during injection, potentially leading to under-dosing.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are affected. Those administering medications with these syringes are most at risk of inaccurate dosing.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part number 58001934). The lot/batch number is 6070801 and UDI-DI is 30886158033562.
Look for Sol-M Luer Lock and Luer Slip 1ml syringes with part number 58001934 in CustomEyes Procedure Packs.
These syringes have a low dead space that can cause inaccurate medication dosing, potentially leading to under-dosing during medical procedures.
Check if your CustomEyes Procedure Packs contain Sol-M Luer Lock and Luer Slip 1ml syringes (part number 58001934). If so, stop using them and contact the manufacturer for alternatives.
The recall notice does not specify a deadline for action.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2926-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2926-2024 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.
