Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000757) due to potential air embolism risk. Affected units sold with 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 could cause air embolism if used improperly, which might lead to serious health issues.
The syringes have a low dead space design that could allow air to enter the bloodstream during injections. This might cause air embolism, a serious condition where air blocks blood flow.
Healthcare professionals using CustomEyes Procedure Packs with specific syringe part numbers are most at risk. Patients receiving procedures using these syringes may also be affected.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part Number 58000757). Affected units have lot numbers 6069002 or 6071184.
Look for Part Number 58000757 on the syringes and lot numbers 6069002 or 6071184 on the packaging.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58000757.
The recall record does not specify a remedy, so check the product details and contact the manufacturer for guidance.
Yes, affected units have lot numbers 6069002 or 6071184.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2821-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2821-2024 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.
