Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584770) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers and batch dates.
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 584770) because these syringes have a low dead space that could lead to inaccurate dosing during medical procedures. This recall affects healthcare professionals and medical facilities using these specific packs.
The syringes have a low dead space, which means they can hold less fluid than intended. This could cause inaccurate dosing of medications or fluids during medical procedures, potentially leading to incorrect treatment.
Healthcare professionals and medical facilities that use CustomEyes Procedure Packs with the specific syringe part number 584770 are most at risk. These packs were sold with the lot/batch number 6067190.
Check for the part number 584770 on the syringe packaging. The affected packs were sold with the lot/batch number 6067190 and may have the UDI-DI code 30886158008973.
Look for the part number 584770 on the syringe packaging or the lot/batch number 6067190 on the pack.
The part number is 584770.
The lot/batch number is 6067190.
Check for the part number 584770 on the syringe packaging or the lot/batch number 6067190 on the pack.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2792-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2792-2024 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.
