Leica Biosystems Richmond Inc.: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: September 20, 2017. Most recent: September 20, 2017.

Risk classification: Class II: 5

Most recent recalls

DateAgencyProduct
September 20, 2017FDACell Marque, Glypican-3 (1G12 Mab), 7 mL, REF PA0800, IVD, The antibody is intended for i…Z-3121-2017
September 20, 2017FDACell Marque, SOX-10 (Polyclonal), 7 mL, REF PA0813, IVD, This antibody is intended for in…Z-3126-2017
September 20, 2017FDACell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended f…Z-3120-2017
September 20, 2017FDACell Marque, PAX8 (MRQ-50 Mab.), 7 mL, REF PA0808, IVD, This antibody is intended for in …Z-3125-2017
September 20, 2017FDACell Marque, Napsin A (MRQ-60 Mab.), 7 mL, REF PA0805, IVD, The antibody is intended fo…Z-3124-2017

Questions about this company

How many recalls does Leica Biosystems Richmond Inc. have?
Recalert has 5 U.S. recalls on record for Leica Biosystems Richmond Inc., published between September 20, 2017 and September 20, 2017.
What was the most recent Leica Biosystems Richmond Inc. recall?
FDA recall Z-3121-2017, published September 20, 2017: Cell Marque, Glypican-3 (1G12 Mab), 7 mL, REF PA0800, IVD, The antibody is intended for in vitro diagnostic (IVD) use. Glypican-3 (1G12) Mouse Monoclonal Primary Antibody is intended for laboratory u…
Which agencies have handled Leica Biosystems Richmond Inc. recalls?
Leica Biosystems Richmond Inc. appears as the recalling firm in recalls from: FDA (5).

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