Ascend Laboratories LLC recalls Olmesartan Medoxomil Tablets, USP, 20 mg, Rx Only, 30 Tablets, Manufactured by Alkem Laboratories Ltd, Mumbai, 400 013.
Ascend Laboratories recalls 20 mg Olmesartan Medoxomil tablets (NDC 67877-446-30) manufactured in India with foreign tablet risk. Stop using if you have the product.
Recall notice
Presence of Foreign Tablet/Capsule
Contact the company & request your remedy
What happened, in plain English
Ascend Laboratories is recalling 20 mg Olmesartan Medoxomil tablets (Rx only) due to a foreign tablet or capsule present. This could cause injury if taken. The recall covers specific batches from India. Read more at govinfonow.com/recall/36164-ascend-laboratories-recalls-olmesartan-medoxomil-tablets-with-foreign-tablet-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36164-ascend-laboratories-recalls-olmesartan-medoxomil-tablets-with-foreign-tablet-risk · Updated October 4, 2026 · FDA enforcement record: FDA #D-0392-2021
Cite this page
“Ascend Laboratories recalls Olmesartan Medoxomil Tablets with foreign tablet risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36164-ascend-laboratories-recalls-olmesartan-medoxomil-tablets-with-foreign-tablet-risk. Based on FDA recall #D-0392-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0392-2021%22&limit=1).
Why it’s dangerous
The product contains a foreign tablet or capsule that could be taken by mistake, leading to potential injury. This is a risk in normal use for people who have the prescription.
Who’s affected
People with a prescription for these tablets in the US who received the product from Ascend Laboratories LLC. Those with the specific batch number (20122548) are most at risk.
How to tell if you have this one
Check for the batch number 20122548 on the product label. The product is a 20 mg Olmesartan Medoxomil tablet (Rx only) with NDC 67877-446-30.
- Brand
Ascend Laboratories- Category
Drug
What to do — step by step
Check Product Label
Look for the batch number 20122548 on the label to confirm if it's recalled.
Questions people ask
Is this product safe to take?
The recall states there is a foreign tablet or capsule present, so it is not safe to take.
How can I tell if I have the recalled product?
Check for the batch number 20122548 on the label. The product is a 20 mg Olmesartan Medoxomil tablet (Rx only) with NDC 67877-446-30.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact your doctor or pharmacist for advice.
Contact Ascend Laboratories
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0392-2021 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0392-2021 from Ascend Laboratories. 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-0392-2021 (April 29, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0392-2021 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.