Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000404) 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 specific Sol-M syringes. These syringes have a low dead space design that could lead to inaccurate medication dosing if used improperly.
The syringes have a low dead space design that may cause inaccurate medication dosing if not properly filled. This could lead to under-dosing in medical procedures.
Users of CustomEyes Procedure Packs with the specified syringes (Part Number 58000404) are affected. Healthcare professionals using these syringes for medical procedures are most at risk.
Check for the Part Number 58000404 on the syringe packaging. The recall includes CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes.
Look for the Part Number 58000404 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall is for CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000404) due to potential low dead space causing inaccurate dosing.
Check the syringe packaging for Part Number 58000404. If found, contact Beaver Visitec for guidance.
The recall indicates a potential for inaccurate dosing, but no specific injury mechanism is described 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-2806-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2806-2024 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.
