Becton Dickinson & Co.: Medical Device Recall in 2021 - (Recall #: Z-0762-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

BD Phoenix PMIC/ID-108: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448608

Product Classification:

Class II

Date Initiated: December 8, 2020

Date Posted: January 6, 2021

Recall Number: Z-0762-2021

Event ID: 86963

Reason for Recall:

BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant SXT result with S. aureus could lead to a potential loss of access to a preferred antibiotic regimen and potential reduction in effectiveness of treatment of the infection

Status: Terminated

Product Quantity: 34825 eaches

Code Information:

All unexpired lots UDI: 00382904486082

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated