Becton Dickinson & Co.: Medical Device Recall in 2019 - (Recall #: Z-0935-2019)

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:

Phoenix AP AST Indicator Bag, Catalog Number 246006

Product Classification:

Class II

Date Initiated: December 20, 2018

Date Posted: March 6, 2019

Recall Number: Z-0935-2019

Event ID: 81952

Reason for Recall:

Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.

Status: Terminated

Product Quantity: 62880 total

Code Information:

Batch Numbers 8234684 8234533 8225579 8225578 8218607 8218605 8213696 8213635 8213633 8208581 8208579 8206585 8190531 8190530 8170557 8234505 8170562 8159691 8150670 8150669

Distribution Pattern:

The products were distributed to the following US states: AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY. The products were distributed to the following foreign countries: Argentina, Australia, Bangladesh, Belgium, Brazil, Canada, Cayman Islands, Chile, China, Columbia, Costa Rica, Dominican Republic, Ecuador, Guatemala, India, Indonesia, Japan, Korea, Malaysia, Mexico, Myanmar, New Zealand, Pakistan, Panama, Peru, Philippines, San Salvador, Singapore, Sri Lanka, Thailand, Taiwan, Uruguay, Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated