Beaver Visitec recalls Malosa Core Phaco Pack 1 medical cataract kits with packaging holes that could compromise sterility. Affected kits have specific part and lot numbers. Consumers should contact the manufacturer for details.
Kit packaging may have small holes compromising product sterility
Beaver Visitec recalls certain Malosa Core Phaco Pack 1 cataract surgery kits because their packaging may have small holes that could allow contamination. This could lead to infections during surgery if the kit is used without proper sterility.
The kit packaging may have small holes that could allow contaminants to enter the sterile packaging. This could lead to infections if the kit is used without proper sterility during surgery.
Medical professionals who use the Malosa Core Phaco Pack 1 cataract kits for surgery are most at risk if the packaging holes compromise sterility during procedures.
Check for part number MMK833/2 and lot numbers 3272267, 3274728, or 3323887 on the packaging. These kits were sold for cataract, corneal, or refractive surgery procedures.
Look for part number MMK833/2 and lot numbers 3272267, 3274728, or 3323887 on the packaging.
Beaver Visitec recalls Malosa Core Phaco Pack 1 cataract surgery kits with packaging that may have small holes, risking contamination during surgery.
Check for part number MMK833/2 and lot numbers 3272267, 3274728, or 3323887 on the packaging.
The recall record does not specify a remedy, so contact Beaver Visitec directly for instructions.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-0407-2022 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-0407-2022 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.
