Becton Dickinson & Co.: Medical Device Recall in 2019 - (Recall #: Z-2322-2019)

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 Cdiff EU; Catalog # 442555

Product Classification:

Class II

Date Initiated: July 17, 2019

Date Posted: August 28, 2019

Recall Number: Z-2322-2019

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: 4 units

Code Information:

Lot # 9127912 ; UDI (GTIN, DI+PI): (01)00382904425555 (17)201114(10)9127912(30)1

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