Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001314) 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 specific syringes from Sol-M. These syringes could pose contamination risks if used incorrectly, potentially leading to infections.
The syringes in question have a low dead space design, which can trap contaminants during use. If not properly cleaned or handled, these syringes may introduce infections into the bloodstream.
Users of CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes (Part Number 58001314) are affected. Healthcare professionals and individuals using these medical devices for procedures are most at risk.
Check for the Part Number 58001314 on the syringe packaging. The product was sold with UDI-DI: 30886158023440 and Lot/Batch Number 6049642.
Look for Part Number 58001314 on the syringe packaging or label.
The Part Number is 58001314.
Check for Part Number 58001314 on the syringe packaging or label.
The recall is due to potential contamination risks, not immediate serious injury. The hazard level is low risk.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2857-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2857-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.