Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001712) 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 58001712) because these syringes have a low dead space design that could cause air embolism if used improperly. This recall affects medical professionals and patients using these syringes for procedures.
These syringes have a low dead space design that could allow air to enter the bloodstream during procedures, potentially causing air embolism if not used correctly. The risk is related to improper handling or use of the syringes in medical procedures.
Medical professionals and patients who use CustomEyes Procedure Packs containing the specific syringes are affected. Those with the Part Number 58001712 syringes are most at risk.
Check for the Part Number 58001712 on the syringes. The syringes are part of Beaver Visitec CustomEyes Procedure Packs sold with specific UDI-DI and Lot/Batch numbers.
Look for Part Number 58001712 on the syringes to confirm if they are affected.
The recall is due to low dead space syringes that could cause air embolism if used improperly during medical procedures.
Check the syringe for Part Number 58001712. If affected, contact Beaver Visitec for guidance.
These syringes have a low dead space design that could allow air to enter the bloodstream, potentially causing air embolism if not used correctly.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2906-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2906-2024 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.
