Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001775) due to potential contamination risks. Affected units include specific lot 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 were manufactured by Sol-M and may have low dead space, which could lead to contamination risks during medical procedures.
The syringes have low dead space, meaning they can hold small amounts of fluid. This design could potentially allow contaminants to enter the syringe during use, increasing the risk of infection or contamination in medical procedures.
Healthcare professionals using CustomEyes Procedure Packs with the specified syringes are likely affected. Patients receiving procedures using these syringes may be at risk if contamination occurs.
Check for the Part Number 58001775 on the syringe packaging. Affected units include specific lot numbers: 6067403 and 6070758.
Look for the Part Number 58001775 on the syringe packaging to identify affected units.
The recall includes Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001775.
Affected lot numbers are 6067403 and 6070758.
The recall does not specify a stop-use instruction; check the packaging for the Part Number to identify affected units.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2913-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2913-2024 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.
