Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001212) due to potential contamination risks. Affected units may have low dead space syringes 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 (Part Number 58001212) because these syringes have a low dead space design that could lead to injection errors if used incorrectly. This recall is important for medical professionals who use these syringes in 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, potentially leading to injection errors.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving injections with these syringes could experience errors if the syringes are not used properly.
Check for the Part Number 58001212 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs sold by Beaver Visitec International, Inc.
Look for the Part Number 58001212 on the syringe packaging to identify affected units.
The recall is due to a low dead space design in the syringes that could lead to injection errors if not used correctly.
Check the syringe packaging for the Part Number 58001212. If you have this number, contact Beaver Visitec for guidance.
The low dead space design could cause inaccurate dosing if the syringe is not properly filled before use, potentially leading to injection errors.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2853-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2853-2024 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.
