NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for daily wear for persons requiring keratoconus management for the correction of refractive ametropia (myopia, hyperopia) in aphakic and not aphakic persons with otherwise nondiseased eyes. The lens may be worn by persons who exhibit refractive astigmatism of 1.50 diopters or less where the astigmatism does not interfere with visual acuity.

Class I - Dangerous
🏥 Medical Devices Recalled: November 3, 2017 Alden Optical Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    AZ154920 AZ154720
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Alden Optical
Reason for Recall:
Contact lenses lack sterility assurance.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for daily wear for persons requiring keratoconus management for the correction of refractive ametropia (myopia, hyperopia) in aphakic and not aphakic persons with otherwise nondiseased eyes. The lens may be worn by persons who exhibit refractive astigmatism of 1.50 diopters or less where the astigmatism does not interfere with visual acuity.

Product Codes/Lot Numbers:

AZ154920 AZ154720

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0981-2018

Related Recalls

Vials labeled for the prescriptions contained incorrect lenses

Jul 3, 2018 Infusion Pumps View Details →

Vials labeled for the prescriptions contained incorrect lenses

Jul 3, 2018 Infusion Pumps View Details →

Contact lenses lack sterility assurance.

Nov 3, 2017 Infusion Pumps Nationwide View Details →