Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part 58001602) due to potential low dead space issues. Affected units sold with specific part numbers and batch codes.
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 which could cause inaccurate dosing during medical procedures. This recall matters because improper dosing could lead to treatment errors.
The syringes have a low dead space design, meaning small amounts of fluid can remain in the syringe after drawing. This could lead to inaccurate dosing if the fluid isn't fully expelled before use. The risk is primarily for medical procedures requiring precise medication delivery.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes may also be affected.
Check for the part number 58001602 on the syringe packaging. Affected packs were sold with specific batch numbers and UDI-DI codes listed in the recall notice.
Look for the part number 58001602 on the syringe packaging or the CustomEyes Procedure Pack label.
The part number is 58001602.
Check for the part number 58001602 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall does not specify a remedy, so you should contact the manufacturer for further instructions.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2887-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2887-2024 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.
