🔍 RecallPedia

ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR

Class I - Dangerous
🏥 Medical Devices Recalled: October 19, 2017 Johnson & Johnson Vision Care Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot B00DHLP Exp. 08/2018 Base Curve 8.7, Refractive Power -10.00D - Manufactured in J&J Vision Care Inc. Jacksonville, FL Lot L002FNL Exp. 07/2020 Base Curve 8.7 Refractive Power -4.75D Manufactured in J&J Vision Care Ireland Lot L002V94 Exp. 01/2022 Base Curve 8.7 Refractive Power -5.00D
  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:
Johnson & Johnson Vision Care, Inc.
Reason for Recall:
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR

Product Codes/Lot Numbers:

Lot B00DHLP Exp. 08/2018 Base Curve 8.7, Refractive Power -10.00D - Manufactured in J&J Vision Care Inc. Jacksonville, FL Lot L002FNL Exp. 07/2020 Base Curve 8.7 Refractive Power -4.75D Manufactured in J&J Vision Care Ireland Lot L002V94 Exp. 01/2022 Base Curve 8.7 Refractive Power -5.00D

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1210-2018

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