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Becton Dickinson & Co. recalls Phoenix AST-s Indicator, Catalog Number 246009
Recalled March 6, 2019 · FDA recall Z-0933-2019 · Becton Dickinson &
Hazard
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts. · FDA Class II
Units
62880 total
Sold at
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
Description
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Product
Phoenix AST-s Indicator, Catalog Number 246009
Manufacturer(s)
Becton Dickinson & Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →