FDAFDA · Food and drugs·Recall number D-0407-2019
Glutathione liquid, 200mg/ml, Rx
Published January 9, 2019 · Recall initiated: January 2, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of sterility assurance.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hiers Enterprises, LLC dba Northwest Compounding Pharmacy
- Distributor
- Product was distributed exclusively in the state of Oregon to 3 Medical facilities, 1 Physician's office and 80 consumers/patients. These are compounded products - labels vary for each compound - specific to each patient. Firm did not provide labeling.
- Lot
- 10092018@5
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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