Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584712) due to potential low dead space issues. Affected units may cause inaccurate dosing if used improperly.
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 584712) because these syringes have a low dead space design that could lead to inaccurate dosing if used incorrectly. This recall affects medical professionals and patients using these syringes for procedures.
The syringes have a low dead space design, which means small amounts of liquid can remain in the syringe after drawing. If the syringe is not properly resealed or used, this could lead to inaccurate dosing of medications or fluids during medical procedures.
Medical professionals and patients who use the CustomEyes Procedure Packs with the specified syringes are most at risk. The recall targets users who may have been given these syringes for medical procedures.
Check for the Part Number 584712 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs manufactured by Beaver Visitec International, Inc.
Look for the Part Number 584712 on the syringe packaging to confirm if the product is affected.
The recall is due to low dead space syringes that could lead to inaccurate dosing if used improperly.
Check the syringe packaging for Part Number 584712. If it matches, contact Beaver Visitec for guidance.
While the risk is low, improper use could lead to inaccurate dosing 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-2789-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2789-2024 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.
