Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001764) due to potential low dead space issues. Affected units may cause inaccurate dosing during medical procedures.
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 syringes from Sol-M. These syringes have a low dead space design which could lead to inaccurate medication dosing during medical procedures.
The syringes have a low dead space design that can cause medication to not fully mix with the solution, potentially leading to inaccurate dosing during medical procedures. This is a risk for medical professionals using the syringes in procedures requiring precise medication delivery.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures with these syringes may experience inaccurate dosing.
Check for the Part Number 58001764 on the syringe packaging. The recall affects CustomEyes Procedure Packs sold with Sol-M Luer Lock and Luer Slip 1ml syringes.
Look for the Part Number 58001764 on the syringe packaging to identify affected units.
The recall is due to low dead space syringes that could cause inaccurate medication dosing during medical procedures.
Check the syringe packaging for Part Number 58001764. If found, contact Beaver Visitec for guidance.
The low dead space design could lead to inaccurate dosing, but the recall is for low-risk medical use cases.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2911-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2911-2024 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.
