Name | Date | Date initiated | Country | Source |
---|---|---|---|---|
Recall of Device Recall Alere iScreen Dx Urine Drug Screen Card | 2017-12-15 | United States | USFDA | |
Recall of Device Recall Dimension Vista Calcium (CA) Flex Reagent cartridge | 2018-01-30 | United States | USFDA | |
Recall of Device Recall MicroVue BAP EIA, Model 8012 | 2016-07-14 | United States | USFDA | |
Recall of Device Recall Atellica IM 1300 Analyzer | 2018-02-26 | United States | USFDA | |
Recall of Device Recall Atellica Solution and Atellica Sample Handler Prime | 2018-02-26 | United States | USFDA |