Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001503) due to potential contamination risks. Affected units may have a low dead space design that could cause injection errors.
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 injection errors if used incorrectly. The recall is for safety reasons to prevent potential harm during medical procedures.
The syringes have a low dead space design, which means air can be trapped inside the syringe barrel. This could cause inaccurate dosing if the syringe is not properly filled before use. The risk is primarily for medical procedures where precise medication delivery is critical.
Medical professionals who use these syringes for procedures are most at risk. Patients receiving injections with these syringes could face errors if the syringes are not properly used.
Check for the part number 58001503 on the syringe packaging. The product was sold with UDI-DI: 30886158024348 and lot number 6069199.
Look for the part number 58001503 on the syringe packaging or the product label.
The recall is due to a low dead space design in the syringes that could lead to injection errors if not used correctly.
Check for the part number 58001503 on the syringe packaging. If you have the product, contact Beaver Visitec for further instructions.
The low dead space design could cause inaccurate dosing during medical procedures, but the risk is low if used correctly.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2877-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2877-2024 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.
