Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584404) 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 584404) 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.
The syringes have a low dead space, meaning small amounts of liquid may remain in the syringe after drawing medication. This could lead to inaccurate dosing if the liquid is not fully expelled before use, potentially causing underdosing in medical procedures.
Healthcare professionals who use CustomEyes Procedure Packs with the specified syringes are most at risk. The recall targets users of these medical devices for procedures requiring precise medication delivery.
Check for the Part Number 584404 on the syringe packaging. The recall includes CustomEyes Procedure Packs that contain Sol-M Luer Lock and Luer Slip 1ml syringes with specific lot/batch numbers.
Look for Part Number 584404 on the syringe packaging to identify affected units.
The recalled syringes have Part Number 584404.
The recall is due to low dead space in the syringes, which could lead to inaccurate medication dosing during procedures.
Check for Part Number 584404 on the syringe packaging or look for the specific lot/batch numbers mentioned in the recall.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2782-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2782-2024 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.
