Alcon Air Optix Night & Day Aqua recall
Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is…
Why was Alcon Air Optix Night & Day Aqua recalled?
Potentially counterfeit products in/and counterfeit packaging were imported to the U.S.
What should I do if I have this product?
Review the official FDA enforcement record for current 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 31202568; 31255298; 31257909; 31229117; 31252252.
- Product
- Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is…
- Recalling firm
- Allied Vision Group Inc
- Quantity
- 655 boxes with 6 units per box. total 3930
- Distribution
- Worldwide and US Nationwide
- Recall date
- May 6, 2020
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)