AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum Quantitative determination of Uric Acid in serum.

Class I - Dangerous
🏥 Medical Devices Recalled: February 11, 2014 AMS Diagnostics Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Numbers: 40147, 80147. Lot codes: 131253, 131254, 131255.
  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:
AMS Diagnostics, LLC
Reason for Recall:
Marketing the devices outside 510(k) requirements
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum Quantitative determination of Uric Acid in serum.

Product Codes/Lot Numbers:

Model Numbers: 40147, 80147. Lot codes: 131253, 131254, 131255.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1268-2014

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