Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use. The Podoplanin (D2-40) antibody is intended for qualified laboratories to qualitatively identify by light microscopy the presence of associated antigens in sections of formalin-fixed, paraffin-embedded tissue sections using IHC test methods

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Product Code PA0796, Lot No. 47793, Exp. Date 09/24/2019
  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:
Leica Biosystems Richmond Inc.
Reason for Recall:
A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use. The Podoplanin (D2-40) antibody is intended for qualified laboratories to qualitatively identify by light microscopy the presence of associated antigens in sections of formalin-fixed, paraffin-embedded tissue sections using IHC test methods

Product Codes/Lot Numbers:

Product Code PA0796, Lot No. 47793, Exp. Date 09/24/2019

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3120-2017

Related Recalls

A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.

Jul 14, 2017 Diagnostic Equipment Nationwide View Details →

A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.

Jul 14, 2017 Diagnostic Equipment Nationwide View Details →

A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.

Jul 14, 2017 Diagnostic Equipment Nationwide View Details →