Becton Dickinson & Co.: Medical Device Recall in 2019 - (Recall #: Z-2323-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Kit BD Max ExK DNA 1 USA; Catalog # 442817

Product Classification:

Class II

Date Initiated: July 17, 2019

Date Posted: August 28, 2019

Recall Number: Z-2323-2019

Event ID: 83406

Reason for Recall:

The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.

Status: Terminated

Product Quantity: 115 units

Code Information:

Lot # 9085666; UDI (GTIN, DI+PI): (01)00382904428174 (17)201024(10)9085666(30)1; Exp: 10/24/2020 Lot #9106886; UDI (GTIN, DI+PI): (01)00382904428174 (17)201107(10)9106886(30)11; Exp: 11/7/2020 Lot #9127935; UDI (GTIN, DI+PI): (01)00382904428174 (17)201130(10)9127935(30)11; Exp: 11/30/2020

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated