A Class I recall has been issued for 24,900 vials of 4.2% sodium bicarbonate injection distributed by Hospira, a Pfizer company, because of the potential presence of glass particulate, according to the November 15, 2023, US Food and Drug...
A Class I recall has been issued for 24,900 vials of 4.2% sodium bicarbonate injection distributed by Hospira, a Pfizer company, because of the potential presence of glass particulate, according to the November 15, 2023, US Food and Drug...
A Class I recall has been issued...