Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58000479) due to potential low dead space causing inaccurate dosing. Affected units sold with specific batch 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. These syringes have a low dead space design that could lead to inaccurate dosing during medical procedures. If you own these packs, stop using them immediately to avoid potential medication errors.
The syringes have a low dead space design that may cause inaccurate medication dosing when used in medical procedures. This could lead to under-dosing or over-dosing of medications depending on the procedure.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing.
Check for the part number 58000479 on the syringe packaging. Affected packs were sold with batch numbers 6071531 or 6073788.
Discontinue use of CustomEyes Procedure Packs containing the specified syringes to prevent potential medication dosing errors.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with part number 58000479.
Check for part number 58000479 on the syringe packaging or batch numbers 6071531 or 6073788 on the label.
Stop using the product immediately to prevent potential medication dosing errors.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2810-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2810-2024 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.
