Kit BD Max MRSA; Catalog # 442953
Check against the official notice below — it lists the full affected range.
Becton Dickinson & Co. is recalling 176 units of the BD MAX MRSA Kit (Catalog #442953, Lot #9071522) because the foil bags containing extraction tubes for BD MAX Reagent products may not have been sealed properly. The affected product has an expiration date of 12/19/2019 and was distributed across multiple U.S. states (including Alabama, Arizona, California, Florida, New York, and Texas, among others) as well as internationally to countries including Australia, Brazil, Canada, Japan, Mexico, and Singapore.
The recall record does not specify a remedy or recommended action for consumers who may have this product.
Written by software from the official notice below. Not reviewed by a lawyer.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Reason for recall: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly. Distribution: 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 Quantity: 176 units Lot/code info: Lot # 9071522; UDI (GTIN, DI+PI): (01)00382904429539 (17)191219(10)9071522(30)1; Exp :12/19/2019
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.