---
title: "Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to be used to... — FDA record Z-0406-2022 | Is It on Recall"
description: "Kit packaging may have small holes compromising product sterility"
url: https://isitonrecall.com/recall/fda-device-z-0406-2022-malosa-core-suface-treatment-pack-medical-corneal-kit-intended-to-be-used-to-aid-in-cataract-corneal/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to be used to aid in cataract, corneal, or refractive... — FDA record Z-0406-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 17, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK110/3
- **Reason**: Kit packaging may have small holes compromising product sterility
- **Classification**: Class II
- **Recalling firm**: Beaver Visitec International, Inc.
- **Quantity**: 380 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0406-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0406-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Numbers: 3347921, 3358240 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

CA, CO, LA, MA, MD, ND, PA, TN, UT

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Utah](https://isitonrecall.com/state/utah/)

## Dates in the source

- **Report date**: Dec 29, 2021
- **Recall initiation date**: Nov 17, 2021
- **Center classification date**: Dec 21, 2021

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0406-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Beaver Visitec International, Inc. records](https://isitonrecall.com/brand/beaver-visitec-international-inc/)