FDAFDA · Food and drugs·Recall number D-1083-2017
Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles (NDC 10702-026-10), Rx only, mfd. by: KVK-TECH, INC. NEWTOWN, PA 18940
Published August 23, 2017 · Recall initiated: August 3, 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 Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PHENTERMINE HYDROCHLORIDE
- Manufacturer
- KVK-Tech, Inc.
- Distributor
- Nationwide in the United States
- UPC
- 0310702027107
- Lot
- Lot # a):12322A, 12323B, 12324A, Exp. Sep 2017; 12455A, Exp. Dec 2017; b) 12323A, Exp. Sep 2017; 12456A, Exp. Dec 2017
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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