Recall Z-0609-2020— Lens.com
Class II · Completed
Class II FDA medical device recall by Lens.com, initiated 2018-08-14. FDA's recall record names no specific 510(k) clearance for this event. 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 Alcon Laboratories, Inc., Fort Worth, TX.. Reason: The product may be counterfeit and could have microbial issues..
- Recalling firm
- Lens.com
- Classification
- Class II
- Status
- Completed
- Initiated
- 2018-08-14
- Firm location
- Las Vegas, NV, United States
Product description
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 Alcon Laboratories, Inc., Fort Worth, TX.
Reason for recall
The product may be counterfeit and could have microbial issues.
Data sourced from openFDA. This site is unofficial and independent of the FDA.