Alden HP49 Sphere Daily Wear Soft contact; Catalog Number: AOHPS49 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia). 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:
    AZ150110 AZ150120 AZ103810 AZ053210 AZ150510 AZ117720 AZ134110 AZ151520 AZ071720 AZ130410 AZ130420
  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:

Alden HP49 Sphere Daily Wear Soft contact; Catalog Number: AOHPS49 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia). 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:

AZ150110 AZ150120 AZ103810 AZ053210 AZ150510 AZ117720 AZ134110 AZ151520 AZ071720 AZ130410 AZ130420

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0984-2018

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 →