Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000455) 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 58000455) because these syringes have a low dead space that could lead to inaccurate medication dosing. This recall matters because improper dosing could cause harm during medical procedures.
The syringes have a low dead space, meaning small amounts of liquid may remain in the syringe after drawing medication. This can cause inaccurate dosing when transferring medication to a patient, potentially leading to underdosing or overdosing.
Medical professionals using CustomEyes Procedure Packs with the specific syringes (Part Number 58000455) are most at risk. Patients receiving treatments with these syringes could experience inaccurate dosing.
Check for the Part Number 58000455 on the syringe packaging. Affected packs were sold with specific batch numbers and dates, including Lot/Batch Number 6062130.
Look for Part Number 58000455 on the syringe packaging or label.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58000455.
Check for Part Number 58000455 on the syringe packaging or label. Affected packs also have Lot/Batch Number 6062130.
The recall does not require immediate stop use; check the part number to confirm if you have the affected product.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2808-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2808-2024 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.
