CLASS II ONGOING Drug recall · Reported 28 May 2025 · FDA Enforcement Report
Phentermine Hydrochloride Capsules, USP 30mg recalled by KVK Tech
KVK Tech is recalling Phentermine Hydrochloride Capsules, USP 30mg, distributed nationwide in the US. The recall was initiated on 9 May 2025 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0446-2025
- FDA event ID
- 96847
- Recalling firm
- KVK Tech, Newtown, PA
- Manufacturer
- KVK-Tech, Inc.
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 9 May 2025
- FDA classified
- 21 May 2025
- Reported
- 28 May 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 9 May 2025 | Recall initiated by company | |
| 21 May 2025 | Classified by FDA | +12 days |
| 28 May 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
cGMP deviations
Product as listed by the FDA
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.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
cGMP deviations
Which lots are affected?
Lot#: 18350A, 18351A, Exp 6/30/2027
Where was it sold?
Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 96847This product is part of a recall event; the main page for the event is Indomethacin Extended-Release Capsules USP, 75 mg recalled by KVK Tech.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Indomethacin Extended-Release Capsules USP, 75 mg recalled by KVK TechIndomethacin | KVK Tech | Manufacturing (CGMP) Deviations | Nationwide |
More recalls from KVK Tech
All 15| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Indomethacin Extended-Release Capsules USP, 75 mg recalled by KVK TechIndomethacin | KVK Tech | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Betaxolol Tablets, USP 10 mg recalled by KVK-TechBetaxolol Hydrochloride | Kvk-Tech | Other | Nationwide |
| Drug | CLASS I | Atovaquone Oral Suspension, USP, 750 mg recalled by KVK-TechAtovaquone Oral Suspension | Kvk-Tech | Temperature Abuse | Nationwide |
| Drug | CLASS III | Hydrocodone Bitartrate and Homatropine Methlybromide recalledHydrocodone Bitartrate And Homatropine Methylbromide | Kvk-Tech | Potency & Assay | Nationwide |
| Drug | CLASS III | Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg recalled | Kvk-Tech | Potency & Assay | Nationwide |
Other Phentermine recalls
All 8| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Phentermine, 30 mg capsules, Rx only recalled by Calvin Scott & Company | Calvin Scott | Potency & Assay | 5 states |
| Drug | CLASS II | Phentermine Hydrochloride Capsules, USP 15mg recalledPhentermine | Aurobindo Pharma USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Phentermine, USP Capsules, 15 mg recalled by Aidarex Pharmaceuticals | Aidarex Pharmaceuticals | Potency & Assay | CA, NV |
| Drug | CLASS III | Phentermine Capsules, 15 mg, a) bottle recalled by PD-Rx PharmaceuticalsPhentermine Hydrochloride | PD-Rx Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Phentermine HCL Capsules, USP 15 mg recalled by KVK-TechPhentermine Hydrochloride | Kvk-Tech | Potency & Assay | Nationwide |