Phentermine Hydrochloride Capsules recalled over manufacturing violations
- Recall date
- May 9, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- KVK Tech, Inc. recalls Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, M…
- Recall number
- D-0446-2025
- FDA classification
- Class II
- Brand / firm
- KVK Tech, Inc.
- Sold / distributed
- Nationwide
Why it was recalled
cGMP deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-028-01.
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