Beaver Visitec recalls Malosa Core Phaco Pack 2 medical kits due to potential packaging holes that could compromise sterility during surgery. Affected units have specific part and lot numbers.
Kit packaging may have small holes compromising product sterility
Beaver Visitec recalls the Malosa Core Phaco Pack 2 medical refractive kits because the packaging might have small holes that could let contaminants in. This could risk infection during surgery if the kit is used without proper sterility.
The packaging may have small holes that could allow contaminants to enter the sterile kit. This could lead to infection during surgery if the kit is used without proper sterility checks.
Medical professionals who use the Malosa Core Phaco Pack 2 kits for cataract, corneal, or refractive surgery are most at risk. Patients receiving these procedures may also be affected if the kit is used without proper sterility.
Check for part number MMK834/1 and lot numbers 3289074 on the packaging. The kits are intended for cataract, corneal, or refractive surgery procedures.
Inspect the packaging for small holes that could compromise sterility.
The recall is for potential packaging holes that could compromise sterility, but the risk is low if the kit is used properly.
Part number MMK834/1 with lot numbers 3289074.
The recall does not require stopping use; check for packaging holes before use.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-0408-2022 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-0408-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.