FDAFDA · Food and drugs·Recall number D-0326-2017
TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21
Published January 11, 2017 · Recall initiated: December 22, 2016
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
Failed Stability Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
- Distributor
- Nationwide
- Lot
- T248H15A, Exp. 08/17
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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