Hetero Labs Limited (Unit V) recalls Losartan Potassium Tablets USP, 50 mg, 90 count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.,
Hetero Labs recalls 50mg Losartan Potassium Tablets with bulging tablets. Rx-only bottles manufactured in India may pose safety risks. Consumers should contact for details.
Lower-risk recall
Failed Tablet/Capsule Specification; complaint of bulging tablet
Contact the company & request your remedy
What happened, in plain English
Hetero Labs is recalling 50mg Losart:an Potassium Tablets that may bulge. This could affect safety if the tablets are taken as directed. The recall is for prescription-only bottles sold in the US. Read more at govinfonow.com/recall/36863-hetero-labs-losartan-tablets-recall-bulging-tablets-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36863-hetero-labs-losartan-tablets-recall-bulging-tablets-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1545-2020
Cite this page
“Hetero Labs Losartan Tablets Recall: Bulging Tablets Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36863-hetero-labs-losartan-tablets-recall-bulging-tablets-risk. Based on FDA recall #D-1545-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1545-2020%22&limit=1).
Why it’s dangerous
Bulging tablets can indicate improper manufacturing, potentially leading to inconsistent drug release. This might affect how the medication works in the body, but does not cause immediate harm.
Who’s affected
Prescription users of Losartan Potassium Tablets 50mg, 90-count bottles. People with high blood pressure who take this medication are most at risk.
How to tell if you have this one
Check for the product name 'Losartan Potassium Tablets USP 50 mg', 90-count bottles, Rx only. Look for batch number LOA19357A and expiration date 09/2021.
- Brand
Hetero Labs- Category
Drug
What to do — step by step
Check Product Details
Look for the batch number LOA19357A and expiration date 09/2021 on the bottle.
Questions people ask
Is this product safe to take?
The recall is for potential manufacturing issues that could affect the tablet's consistency, but the product is still safe to take if it's not bulging.
How do I know if I have the recalled product?
Check for the batch number LOA19357A and expiration date 09/2021 on the 90-count prescription bottle.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact the manufacturer for further instructions.
Contact Hetero Labs
We’ve drafted a message you can send Hetero Labs to request your refund or repair — edit it as you like.
Subject: Recall D-1545-2020 — Hetero Labs Hetero Labs Hello, I own a Hetero Labs that is covered by recall D-1545-2020 from Hetero Labs. 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-1545-2020 (August 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1545-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.