Three of the recalls, which BD announced on Aug. 4, 2020, have been designated as Class I recalls by the U.S. Food and Drug Administration (FDA), which means that FDA has determined that there is a reasonable probability that the use of the product will cause serious adverse health consequences or d

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-announces-fda-classifications-august-4th-recalls-bd-alaristm-system-hardware-keypads-incorrect