Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584727) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part 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 (Part Number 584727) because these syringes have a low dead space that could lead to inaccurate dosing during medical procedures. This recall is important for healthcare providers using these syringes as they may receive incorrect medication amounts.
These syringes have a low dead space, meaning small amounts of liquid may remain in the syringe after drawing medication. This can cause inaccurate dosing if the syringe is not properly filled, potentially leading to incorrect medication amounts being administered.
Healthcare providers who use CustomEyes Procedure Packs with the specific syringes (Part Number 584727) are most at risk. Patients receiving treatments with these syringes could potentially receive inaccurate dosing.
Check for Part Number 584727 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs sold with specific lot/batch numbers and UDI-DI codes.
Look for Part Number 584727 on the syringe packaging to identify affected units.
The specific part number for the recalled syringes is 584727.
Check for Part Number 584727 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs with specific lot/batch numbers and UDI-DI codes.
The recall record does not specify a remedy, so you should contact Beaver Visitec for guidance.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2790-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2790-2024 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.
