KVK Tech Phentermine Capsules Recall: Impurities Risk Serious Injury
KVK Tech recalls 100-count and 1000-count 15mg Phentermine capsules due to impurities found in stability testing. These capsules may pose a risk of serious injury if taken.
Lower-risk recall
Failed Impurities/Degradation Specifications: out-of-specification results obtained for individual unknown impurities found at 30 month Room Temperature Retained Sample stability test.
Contact the company
What happened, in plain English
KVK Tech is recalling 15mg Phentermine HCL capsules that were found to have impurities in stability tests. This could lead to serious health risks if taken as directed. Read more at govinfonow.com/recall/41413-kvk-tech-phentermine-capsules-recall-impurities-risk-serious-injury.
Source Summary by GovInfoNow · govinfonow.com/recall/41413-kvk-tech-phentermine-capsules-recall-impurities-risk-serious-injury · Updated October 7, 2026 · FDA enforcement record: FDA #D-1083-2017
Cite this page
“KVK Tech Phentermine Capsules Recall: Impurities Risk Serious Injury.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41413-kvk-tech-phentermine-capsules-recall-impurities-risk-serious-injury. Based on FDA recall #D-1083-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1083-2017%22&limit=1).
Why it’s dangerous
The capsules failed stability tests showing unknown impurities at 30 months when stored at room temperature. These impurities could cause serious health issues if taken.
Who’s affected
People who own or use the recalled 100-count or 1000-count 15mg Phentermine capsules. Those with medical conditions requiring weight management are most at risk.
How to tell if you have this one
Check for 100-count bottles (NDC 10702-026-01) or 1000-count bottles (NDC 10702-026-10) with lot numbers 12322A, 12323B, 12324A, 12455A, 12456A, or 12323A. The capsules are prescription-only and expire by September 2017 or December 2017.
- Brand
KVK Tech- Category
Drug
What to do — step by step
Check Product Details
Identify the product by checking the lot number and expiration date on the bottle.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 16 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1083-2017 (August 3, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1083-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.