Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000910) 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 that could lead to inaccurate medication dosing during medical procedures.
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 the CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures with these syringes could experience inaccurate dosing.
Check for the Part Number 58000910 on the syringes. The product was sold with the UDI-DI 30886158021545 and Lot/Batch Number 6062356.
Look for the Part Number 58000910 on the syringes to confirm if they are affected.
The recall is due to low dead space syringes that may cause inaccurate medication dosing during medical procedures.
The official recall notice does not specify a remedy or action steps for affected products.
Check for the Part Number 58000910 on the syringes, as well as the UDI-DI 30886158021545 and Lot/Batch Number 6062356.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2832-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2832-2024 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.
