Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000759) due to potential contamination risks. Affected units may cause infection if used improperly.
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 specific syringes from Sol-M. These syringes could pose contamination risks if used incorrectly, potentially leading to infections.
The syringes have a potential for contamination due to manufacturing issues with the low dead space design and luer slip tips. If used improperly, they could lead to infections in medical procedures.
Medical professionals and patients using the CustomEyes Procedure Packs with the specified syringes are most at risk. The recall affects units sold with Part Number 58000759.
Check for the Part Number 58000759 on the syringe packaging. The recall includes CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes.
Look for Part Number 58000759 on the syringe packaging to confirm if your CustomEyes Procedure Packs are affected.
The recall is due to potential contamination risks from the syringes' manufacturing process, which could lead to infections if used improperly.
Check for Part Number 58000759 on the syringe packaging. If you have the affected product, contact Beaver Visitec for guidance.
The recall states potential contamination risks, but no specific serious injury mechanism is mentioned. The hazard level is low risk.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2822-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2822-2024 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.
