Becton Dickinson & Co.: Medical Device Recall in 2024 - (Recall #: Z-2585-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;

Product Classification:

Class II

Date Initiated: July 9, 2024

Date Posted: August 21, 2024

Recall Number: Z-2585-2024

Event ID: 94965

Reason for Recall:

There is a potential risk that the image colony count does not adequately reflect the actual plate colony count and may lead to inaccurate counts that would impact patient diagnosis and subsequent care.

Status: Ongoing

Product Quantity: 23 units

Code Information:

Catalog (Ref): 444900; UDI-DI: 00382904449001; Serial Numbers: IA00084, IA00054, IA00055, IA00088, IA00041, IA00071, IA00085, IA00007, IA00014, IA00005, IA00053, IA00073, IA00081, IA00011, IA00012, IA00027, SL01023, IA00026, IA00050, IA00034, IA00025, IA00086, IA00108,

Distribution Pattern:

US distribution to states of: CO, CT, IA, IL, KY, MD, MI, MN, NC, NJ, NY, OH, OK, SC, TN, TX and WA.

Voluntary or Mandated:

Voluntary: Firm initiated