FDAFDA · Food and drugs·Recall number D-1162-2017
Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG: KVK-TECH INC. Newtown. PA --- 33261-0361-30
Published September 20, 2017 · Recall initiated: September 5, 2017
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 Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at the 30 month Room Temperature Retained Sample stability test
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Aidarex Pharmaceuticals LLC
- Distributor
- Distributed to the state of CA and NV.
- Lot
- Batch 47262-2, 47262-3, exp 8/31/2017; 47262-4, exp 12/30/17, 47262-5, 47262-6, 47262-7, exp 12/31/17
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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