Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000603) due to potential low dead space issues. Affected units may cause 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. These syringes have a low dead space design that could lead to inaccurate dosing during medical procedures.
The syringes have a low dead space design, which means small amounts of fluid can remain in the syringe after drawing. This could lead to inaccurate dosing when administering medication or fluids. The risk is primarily for medical procedures where precise measurements are critical.
Medical professionals using CustomEyes Procedure Packs with the specific syringe part numbers are most at risk. Patients receiving treatments with these syringes may experience inaccurate dosing.
Check for the part number 58000603 on the syringe packaging. The product was sold with UDI-DI: 30886158019436 and lot number 6069800.
Look for the part number 58000603 on the syringe packaging or label.
The part number is 58000603.
Check for the part number 58000603 on the syringe packaging or label.
The recall does not specify a fix; affected users should check the syringes and contact the manufacturer if needed.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2816-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2816-2024 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.
