Aidarex Pharmaceuticals LLC recalls Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG:
Aidarex Pharmaceuticals recalls 15mg phentermine capsules with impurities that could cause serious harm. Affected batches expire by 2017. Consumers should contact the company for details.
Recall notice
Failed Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at the 30 month Room Temperature Retained Sample stability test
Contact the company & request your remedy
What happened, in plain English
Aidarex Pharmaceuticals is recalling 15mg phentermine capsules due to impurities that could cause serious harm. This affects specific batches from 2016-2017. The recall is for prescription-only medication. Read more at govinfonow.com/recall/41260-aidarex-phentermine-capsules-15mg-recall-impurities-risk-serious-harm.
Source Summary by GovInfoNow · govinfonow.com/recall/41260-aidarex-phentermine-capsules-15mg-recall-impurities-risk-serious-harm · Updated October 7, 2026 · FDA enforcement record: FDA #D-1162-2017
Cite this page
“Aidarex Phentermine Capsules 15mg Recall: Impurities Risk Serious Harm.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41260-aidarex-phentermine-capsules-15mg-recall-impurities-risk-serious-harm. Based on FDA recall #D-1162-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1162-2017%22&limit=1).
Why it’s dangerous
The capsules failed stability tests showing impurities that could be harmful. These impurities may cause serious health effects if the medication is taken.
Who’s affected
Prescription holders of the specific batch numbers listed. Those with the 15mg phentermine capsules from Aidarex Pharmaceuticals are most at risk.
How to tell if you have this one
Check for batch numbers 47262-2 through 47262-7 on the bottle. The capsules are prescription-only and expire by 2017.
- Brand
Aidarex Pharmaceuticals- Category
Drug
What to do — step by step
Check Batch Number
Look for batch numbers 47262-2 through 47262-7 on the bottle label.
Questions people ask
What is the hazard with these capsules?
The capsules failed stability tests showing impurities that could cause serious health effects.
Which batches are affected?
Batches 47262-2, 47262-3, 47262-4, 47262-5, 47262-6, and 47262-7.
How do I know if I have the recalled product?
Check the batch number on the bottle label; affected batches are 47262-2 through 47262-7.
Contact Aidarex Pharmaceuticals
We’ve drafted a message you can send Aidarex Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1162-2017 — Aidarex Pharmaceuticals Aidarex Pharmaceuticals Hello, I own a Aidarex Pharmaceuticals that is covered by recall D-1162-2017 from Aidarex Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1162-2017 (September 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1162-2017 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.