🔍 RecallPedia

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002

Class I - Dangerous
🏥 Medical Devices Recalled: July 27, 2021 Contamac Solutions Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Number: FOE
  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:
Contamac Solutions, Inc.
Reason for Recall:
Contact lens solution may contain foreign material
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002

Product Codes/Lot Numbers:

Lot Number: FOE

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0030-2022

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