Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584785) 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 584785) because these syringes have a low dead space that could lead to inaccurate dosing during medical procedures. This recall affects healthcare professionals and patients using these specific packs for medical injections.
The syringes have a low dead space, which means they may not hold the full volume of liquid intended for medical use. This can lead to inaccurate dosing during injections, potentially causing under-dosing of medications. However, the risk is not severe enough to cause serious injury in normal use.
Healthcare professionals and patients who use CustomEyes Procedure Packs with the specified syringes (Part Number 584785) are most at risk. The recall targets users who have purchased these packs with the affected syringes.
Check for the Part Number 584785 on the syringe packaging or the CustomEyes Procedure Pack label. The lot/batch number 6075214 and UDI-DI 30886158009000 are also associated with these affected units.
Look for the Part Number 584785 on the syringe packaging or CustomEyes Procedure Pack label.
The specific part number for the recalled syringes is 584785.
Check for the Part Number 584785 on the syringe packaging or the CustomEyes Procedure Pack label. The lot/batch number 6075214 and UDI-DI 30886158009000 are also associated with these affected units.
The recall record does not specify a remedy or fix for these 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-2793-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2793-2024 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.
