PD-Rx Phentermine Capsules 15mg Recall: Impurities May Cause Harm
PD-Rx Pharmaceuticals recalls 15mg Phentermine Capsules due to impurities detected in stability testing. Affected bottles have specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
Recall notice
Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
Contact the company
What happened, in plain English
PD-Rx Pharmaceuticals is recalling 15mg Phentermine Capsules from specific bottle counts and NDC numbers because impurities were found in stability tests. This could pose a risk to health if the capsules are taken as directed. Read more at govinfonow.com/recall/41395-pd-rx-phentermine-capsules-15mg-recall-impurities-may-cause-harm.
Source Summary by GovInfoNow · govinfonow.com/recall/41395-pd-rx-phentermine-capsules-15mg-recall-impurities-may-cause-harm · Updated October 7, 2026 · FDA enforcement record: FDA #D-1118-2017
Cite this page
“PD-Rx Phentermine Capsules 15mg Recall: Impurities May Cause Harm.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41395-pd-rx-phentermine-capsules-15mg-recall-impurities-may-cause-harm. Based on FDA recall #D-1118-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1118-2017%22&limit=1).
Why it’s dangerous
The recall is based on stability testing showing impurities at 30th month room temperature. This means the capsules may contain harmful substances that could affect health if taken as intended.
Who’s affected
People who purchased the recalled Phentermine Capsules from PD-Rx Pharmaceuticals, including those with specific bottle counts and NDC numbers. Those using the medication for weight loss are most at risk.
How to tell if you have this one
Check for the product names and NDC numbers: 7-count (NDC 55289-791-07), 14-count (NDC 55289-791-14), 21-count (NDC 55289-791-21), 30-count (NDC 55289-791-30), or 60-count (NDC 55289-791-60) bottles. Also check the expiration dates listed on the packaging.
- Brand
PD-Rx Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Identify the bottle count and NDC number to confirm if your product is recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.5 years 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-1118-2017 (August 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1118-2017 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.