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Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity 500 Cards and Foil Bags REF CMT01/F02 IFU: Advance Dx 100 SSE(Serum Separating Extraction) Technology BLOOD COLLECTION INSTRUCTIONS

Class I - Dangerous
🏥 Medical Devices Recalled: July 6, 2021 Advance Dx Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Catalog Number: CMT01 GTIN: 1061C010890976 Lot Number: PPD02102 V6
  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:
Advance Dx, Inc.
Reason for Recall:
Due to high glucose test results when using the blood collection cards.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity 500 Cards and Foil Bags REF CMT01/F02 IFU: Advance Dx 100 SSE(Serum Separating Extraction) Technology BLOOD COLLECTION INSTRUCTIONS

Product Codes/Lot Numbers:

Product Catalog Number: CMT01 GTIN: 1061C010890976 Lot Number: PPD02102 V6

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2237-2021