Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA…
Reason Lack of Assurance of Sterility.
113 FDA recalls mention Bicarbonate. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Bicarbonate.
Reason Lack of Assurance of Sterility.
Reason Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.
Reason Lack of Assurance of Sterility
Reason Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Reason Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Reason Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Reason Subpotent Drug: Out of specification for assay
Reason Presence of Particulate Matter; identified as glass
Reason Presence of Particulate Matter; identified as glass
Reason Presence of Particulate Matter: Silicone
Reason Presence of Particulate Matter: identified as glass.
Reason Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Reason Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Reason Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Reason Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Reason Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Reason Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of assurance of sterility.
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.