Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584003) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers and batch codes.
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 584003) because these syringes have a low dead space that could lead to inaccurate medication dosing. This recall affects healthcare professionals using these syringes for procedures.
The syringes have a low dead space, meaning a small amount of fluid may remain in the syringe after drawing medication. This could cause inaccurate dosing if the fluid is not properly accounted for during administration.
Healthcare professionals who use CustomEyes Procedure Packs with the specific syringes (Part Number 584003) are most at risk. Patients receiving treatments with these syringes may also be affected.
Check for the Part Number 584003 on the syringe packaging. Affected packs were sold with specific batch numbers (6063717) and UDI-DI codes (30886158141496).
Look for Part Number 584003 on the syringe packaging to identify affected units.
The specific part number for the recalled syringes is 584003.
Check for Part Number 584003 on the syringe packaging or look for batch number 6063717 and UDI-DI code 30886158141496.
The recall record does not mention any remedy or fix for the recalled syringes.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2781-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2781-2024 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.
