Beaver Visitec recalls Malosa Core Suface Treatment Pack for possible sterility issues due to packaging holes. Affected units include specific part numbers and lot numbers.
Kit packaging may have small holes compromising product sterility
Beaver Visitec recalls its Malosa Core Suface Treatment Pack medical corneal kits because packaging may have small holes that could compromise product sterility. This risk could lead to infections during surgery if the kit is used without proper sterility.
The kit packaging may have small holes that could allow contamination, potentially leading to infections during surgery. This is a sterility risk that could affect the safety of the medical procedure.
Medical professionals who use the Malosa Core Suface Treatment Pack for cataract, corneal, or refractive surgery are likely affected. Patients undergoing these procedures are at risk if the kit is used with compromised sterility.
Check for part number MMK110/3 and lot numbers 3347921 or 3358240 on the packaging. The product is intended for use in cataract, corneal, or refractive surgery.
Look for part number MMK110/3 and lot numbers 3347921 or 3358240 on the packaging.
The Malosa Core Suface Treatment Pack is a medical corneal kit used for cataract, corneal, or refractive surgery.
The packaging may have small holes that could compromise product sterility, potentially leading to infections during surgery.
Check for part number MMK110/3 and lot numbers 3347921 or 3358240 on the packaging. No specific action is required beyond checking.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-0406-2022 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-0406-2022 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.
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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.
