FDAFDA · Food and drugs·Recall number Z-2337-2019
Kit BD Max Enteric Viral Panel RUO; Catalog # 443715
Published August 28, 2019 · Recall initiated: July 17, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Becton Dickinson & Co.
- Distributor
- AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV Worldwide: Australia, Belgium, Brazil, Canada, Chile, China, Hong Kong, Japan, Korea, Mexico, Singapore, Taiwan
- Lot
- Lot # 9114647; UDI (GTIN, DI+PI): (01)00382904437152 (17)201107(10)9114647(30)1; Exp: 11/7/2020
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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