Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part 58000775) due to potential low dead space issues. Affected units sold with specific lot 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 58000775) because these syringes have a low dead space design that could cause inaccurate dosing during medical procedures. This recall matters because improper dosing could lead to treatment errors if used incorrectly.
The syringes have a low dead space design, which means small amounts of fluid can remain in the syringe after drawing medication. This could lead to inaccurate dosing if the fluid isn't fully expelled before administration, potentially causing treatment errors.
Healthcare professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes may also be affected if the procedure is performed incorrectly.
Check for the part number 58000775 on the syringe packaging. The lot number 6070132 and UDI-DI code 30886158020319 are also associated with affected units.
Look for the part number 58000775 on the syringe packaging to identify affected units.
The part number is 58000775.
The lot number is 6070132.
Check for the part number 58000775 on the syringe packaging, or look for the lot number 6070132 and UDI-DI code 30886158020319.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2823-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2823-2024 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.
