Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000195) due to potential contamination risks. Affected units may cause infection if used improperly.
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 contamination if not used correctly, posing a risk of infection.
The syringes have a low dead space design that can trap small amounts of fluid, potentially leading to contamination if not properly cleaned or handled. This could increase the risk of infection during medical procedures.
Healthcare professionals and patients using the CustomEyes Procedure Packs with the specified syringes are likely affected. Those using the syringes for injections or procedures are at higher risk of contamination.
Check for the Part Number 58000195 on the syringe packaging. The product was sold with UDI-DI: 30886158009765 and Lot/Batch Number 6071454.
Look for the Part Number 58000195 on the syringe packaging or the CustomEyes Procedure Pack label.
The Part Number is 58000195.
Check for the Part Number 58000195 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall does not specify a remedy, so no action is required beyond checking if the product is affected.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2801-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2801-2024 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.
