Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001306) due to potential air embolism risk from low dead space syringes.
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 (Part Number 58001306) because these syringes have a low dead space design that could cause air embolism if used improperly. This recall is important for medical professionals who use these syringes for procedures requiring precise fluid measurement.
The syringes have a low dead space design that could allow air to enter the bloodstream during procedures, potentially causing air embolism. This risk is higher when the syringes are used for procedures requiring precise fluid measurement where air entry could be critical.
Medical professionals who use CustomEyes Procedure Packs containing the specified syringes are most at risk. Patients using these syringes for procedures may also be affected if the syringes are used incorrectly.
Check for the Part Number 58001306 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs manufactured by Beaver Visitec.
Look for the Part Number 58001306 on the syringe packaging to identify affected units.
The Part Number is 58001306.
These syringes have a low dead space design that could cause air embolism if used improperly during medical procedures.
Check for the Part Number 58001306 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs manufactured by Beaver Visitec.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2856-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2856-2024 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.
