Oxford Pharmaceuticals, LLC recalls BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle, Rx only, Manufactured By: Oxford Pharmaceuticals, LLC
Oxford Pharmaceuticals recalls 15mg BusPIRone Hydrochloride tablets (NDC 69584-093-10) because foreign tablets may be present. This is a prescription-only product.
Lower-risk recall
Presence of Foreign Tablets/Capsules
Contact the company & request your remedy
What happened, in plain English
Oxford Pharmaceuticals is recalling 15mg BusPIRone Hydrochloride tablets (100-count bottles) because foreign tablets or capsules may be present. This could lead to unintended medication intake if the foreign items are taken. Read more at govinfonow.com/recall/36154-oxford-pharmaceuticals-recalls-buspirone-15mg-tablets-due-to-foreign-tablets.
Source Summary by GovInfoNow · govinfonow.com/recall/36154-oxford-pharmaceuticals-recalls-buspirone-15mg-tablets-due-to-foreign-tablets · Updated October 4, 2026 · FDA enforcement record: FDA #D-0602-2021
Cite this page
“Oxford Pharmaceuticals recalls BusPIRone 15mg tablets due to foreign tablets.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36154-oxford-pharmaceuticals-recalls-buspirone-15mg-tablets-due-to-foreign-tablets. Based on FDA recall #D-0602-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0602-2021%22&limit=1).
Why it’s dangerous
Foreign tablets or capsules may be present in the product. If these foreign items are taken with the intended medication, it could lead to unintended medication intake. This is a prescription-only product, so patients should follow their doctor's instructions.
Who’s affected
Prescription patients who have the 15mg BusPIRone Hydrochlor:ide tablets (NDC 69584-093-10) from Oxford Pharmaceuticals. Patients who take the medication as prescribed are most at risk if foreign tablets are accidentally ingested.
How to tell if you have this one
Check for the product name 'BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle' with NDC 69584-093-10. The product was manufactured by Oxford Pharmaceuticals in Birmingham, Alabama.
- Brand
Oxford Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Verify the product name and NDC number (69584-093-10) to confirm if you have the recalled item.
Questions people ask
Is this product safe to use?
The recall states foreign tablets may be present, but the product is safe if the foreign items are not taken. Consult your doctor if you have concerns.
How can I tell if I have the recalled product?
Check for the product name 'BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle' with NDC 69584-093-10.
What should I do if I have the recalled product?
The recall does not specify a remedy, so check with your doctor or pharmacist for advice.
Contact Oxford Pharmaceuticals
We’ve drafted a message you can send Oxford Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0602-2021 — Oxford Pharmaceuticals Oxford Pharmaceuticals Hello, I own a Oxford Pharmaceuticals that is covered by recall D-0602-2021 from Oxford 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-0602-2021 (May 5, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0602-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.