🔍 RecallPedia

Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25

Class I - Dangerous
🏥 Medical Devices Recalled: November 22, 2024 Nipro Renal Soultions USA Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Model Number: DCA+225-25. Lot Numbers: NDC4F001, NDC4G006, NDC4H009, NDC4H010.
  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:
Nipro Renal Soultions USA, Corporation
Reason for Recall:
The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25

Product Codes/Lot Numbers:

Model Number: DCA+225-25. Lot Numbers: NDC4F001, NDC4G006, NDC4H009, NDC4H010.

Distribution:

Distributed in: US, AZ, FL, GA, IL, MI, NC, NJ, OH, TN, TX

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0820-2025

Related Recalls