Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000056) 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 low dead space design that could allow air to enter the bloodstream during injections, potentially causing air embolism. This risk is specific to medical procedures involving these syringes.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures with these syringes may also be affected.
Check for the Part Number 58000056 on the syringes. The lot numbers 6065306 and 6069372 are also associated with this recall.
Look for the Part Number 58000056 on the syringes and check if the lot numbers 6065306 or 6069372 match.
The recall is due to potential air embolism risk from the low dead space syringes during medical procedures.
Check the Part Number and lot numbers on the syringes to see if they match the recalled items. If they do, contact Beaver Visitec for further instructions.
The recall indicates a potential risk, but the syringes are generally safe unless used improperly during medical procedures.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2795-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2795-2024 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.
