Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in transit may have contributed to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Leica Biosystems Richmond Inc. directly.
Affected Products
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
Quantity: 4
Why Was This Recalled?
A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Leica Biosystems Richmond Inc.
Leica Biosystems Richmond Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report