Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001501) due to potential air embolism risk. 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. These syringes could cause air embolism if used improperly, which may lead to serious health issues.
The syringes have a low dead space design that may allow air to enter the bloodstream during injections. This could cause air embolism, a serious condition where air blocks blood flow.
Medical professionals using CustomEyes Procedure Packs with specific syringe part numbers are most at risk. Patients receiving procedures using these syringes could also be affected.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes. Look for part number 58001501 on the packaging or label. Affected units were sold with specific lot numbers: 6059497 and 6059849.
Look for part number 58001501 on the syringe packaging or label to identify affected units.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with part number 58001501.
Affected units have lot numbers 6059497 and 6059849.
Check for part number 58001501 on the syringe packaging or label. Affected units were sold with specific lot numbers: 6059497 and 6059849.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2876-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2876-2024 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.
