FDA recall record

Beaver Visitec International Malosa Core SMILE Pack 2-Beaver-Visitec- A Medical Refractive recall — FDA Z-0410-2022

Kit packaging may have small holes compromising product sterility

Class IIclassification
Z-0410-2022official record ID
Dec 29, 2021report date

Recall record at a glance

Official recordZ-0410-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeaver Visitec International, Inc.
Report dateDec 29, 2021
Recall initiation dateNov 17, 2021
Quantity1170 units
LocationWaltham, MA, United States

Official product description

Malosa Core SMILE Pack 2-Beaver-Visitec- A Medical Refractive Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK967

Why the product was recalled

Kit packaging may have small holes compromising product sterility

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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