Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000873) due to potential air embolism risk 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 could cause air embolism if used improperly during medical procedures.
The syringes have a potential risk of air embolism if air enters the bloodstream during injection. This could happen if the syringe is not properly sealed or used incorrectly.
Healthcare professionals using these syringes for medical procedures are most at risk. Patients receiving procedures with these syringes may also be affected.
Check for the Part Number 58000873 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs sold with specific lot/batch numbers: 6062129 and 6074045.
Look for the Part Number 58000873 on the syringe packaging to identify affected units.
The recall is for syringes that could potentially cause air embolism if used improperly during medical procedures.
Check the syringe packaging for Part Number 58000873 to identify affected units. Contact Beaver Visitec for further instructions.
The syringes have a potential risk of air embolism if air enters the bloodstream during injection, which could cause serious complications.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2831-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2831-2024 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.
