Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000126) due to potential air embolism risk. Affected units sold with specific batch 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 may have a low dead space design that could cause air embolism if used improperly.
The syringes have a low dead space design that could allow air to enter the bloodstream during injections, potentially causing air embolism. This risk is higher when the syringes are used with certain medical procedures.
Healthcare professionals using CustomEyes Procedure Packs with specific batch numbers of syringes. Patients receiving procedures using these syringes may be at risk if air embolism occurs.
Check for the Part Number 58000126 on the syringe packaging. Affected units include batches 6061650 and 6072066.
Look for the Part Number 58000126 on the syringe packaging or label.
The recall is due to potential air embolism risk from the low dead space design of the syringes.
Check the syringe packaging for Part Number 58000126 and batch numbers 6061650 or 6072066. If affected, contact Beaver Visitec for instructions.
The low dead space design could allow air to enter the bloodstream during injections, potentially causing air embolism.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2797-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2797-2024 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.
