Recall of Alaris Syringe and Alaris PCA Modules by BD CareFusion 303 (Becton, Dickinson and Company) due to potential incorrect display of syringe types and/or sizes.
More on the FDA website .
Recall of Alaris Syringe and Alaris PCA Modules by BD CareFusion 303 (Becton, Dickinson and Company) due to potential incorrect display of syringe types and/or sizes.
More on the FDA website .