Leica Biosystems Richmond Inc. recalls Cell Marque, SOX-10 (Polyclonal), 7 mL, REF PA0813, IVD, This antibody is intended for in vitro diagnostic (IVD) use. S…
- Recall date
- July 14, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-3126-2017
- FDA classification
- Class II
- Brand / firm
- Leica Biosystems Richmond Inc.
- Sold / distributed
- Nationwide Distribution to AR, AZ, CA, CT, FL, GA, IL, IN, KY, LA, MI, MN, NC, NH, NV, NY, OR, PA, SC, TN, TX, VA, and WI.
Why it was recalled
A delay in transit may have contributed to nonconformity as the product was stored outside of defined shipping and handling temperature requirements.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Cell Marque, SOX-10 (Polyclonal), 7 mL, REF PA0813, IVD, This antibody is intended for in vitro diagnostic (IVD) use. SOX-10 Rabbit Polyclonal Primary Antibody is intended for laboratory use in the detection of the SOX-10 protein in formalin-fixed, paraffin-embedded tissue stained in qualitative immunohistochemistry (IHC) testing..
Get recall alerts
Free email alert whenever Leica Biosystems Richmond Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Leica Biosystems Richmond Inc.