Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na…
Reason Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
78 FDA recalls mention Glutathione. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Glutathione.
Reason Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of assurance of sterility.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of assurance of sterility for injectables and solutions intended to be sterile.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Reason Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Reason Lack of sterility assurance.
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