Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000287) 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. These syringes have a low dead space design that could lead to inaccurate dosing if used incorrectly, potentially causing medication errors.
The syringes have a low dead space design that can cause medication to not be fully expelled from the syringe, leading to inaccurate dosing. This could result in under-dosing medication if the syringe is not properly used.
Users of CustomEyes Procedure Packs with the specific syringe part number 58000287 are affected. Healthcare professionals and patients using these syringes for medical procedures are most at risk of inaccurate dosing.
Check for the part number 58000287 on the syringe packaging. The product was sold with UDI-DI: 30886158013182 and lot number 6073793.
Look for the part number 58000287 on the syringe packaging to confirm if it's affected.
The part number is 58000287.
Check for the part number 58000287 on the syringe packaging or the UDI-DI: 30886158013182 and lot number 6073793.
The recall does not require stopping use; affected units should be checked for the part number.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2803-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2803-2024 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.
