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 - DangerousWhat Should You Do?
- Check if you have this product: AZ150110 AZ150120 AZ103810 AZ053210 AZ150510 AZ117720 AZ134110 AZ151520 AZ071720 AZ130410 AZ130420
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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.govFDA Recall Number: Z-0984-2018
Related Recalls
Vials labeled for the prescriptions contained incorrect lenses
Vials labeled for the prescriptions contained incorrect lenses
Contact lenses lack sterility assurance.