Malosa Core Suface Treatment Pack -Medical Corneal Kit recall: Sterility Concern
Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK110/3
Why was Malosa Core Suface Treatment Pack -Medical Corneal Kit recalled?
Kit packaging may have small holes compromising product sterility
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: 3347921, 3358240
- 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
- Recalling firm
- Beaver Visitec International, Inc.
- Quantity
- 380 units
- Distribution
- CA, CO, LA, MA, MD, ND, PA, TN, UT
- Recall date
- December 29, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)