🔍 RecallPedia

Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes.

Class I - Dangerous
🏥 Medical Devices Recalled: September 21, 2012 sanofi-aventis US Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    n/a
  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:
sanofi-aventis US, Inc.
Reason for Recall:
Diamigo, a software application, was released through the i-Phone Global Store which inadvertently allowed global access to the application as opposed to the original intended restriction of access to Brazil.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes.

Product Codes/Lot Numbers:

n/a

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0609-2013

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