Hetero Labs, Ltd. - Unit III recalls Indomethacin Capsules, USP, 50 mg, 100-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.,
Hetero Labs recalls 50mg indomethacin capsules that may be deformed, clumped, or melted. These prescription capsules were manufactured for Camber Pharmaceuticals and sold in the US. Consumers should check product details and contact the manufacturer for a remedy.
Lower-risk recall
Failed Tablet/Capsule Specifications: customer complaints of deformed, clumped, misshaped, melted or stuck together capsules.
Contact the company & request your remedy
What happened, in plain English
Hetero Labs is recalling 50mg indomethacin capsules that customers reported as deformed, clumped, or melted. This issue could affect the capsule's effectiveness and safety for medical use. Read more at govinfonow.com/recall/40340-hetero-labs-indomethacin-capsules-recall-deformed-or-melted-capsules.
Source Summary by GovInfoNow · govinfonow.com/recall/40340-hetero-labs-indomethacin-capsules-recall-deformed-or-melted-capsules · Updated October 6, 2026 · FDA enforcement record: FDA #D-1019-2018
Cite this page
“Hetero Labs Indomethacin Capsules Recall: Deformed or Melted Capsules.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40340-hetero-labs-indomethacin-capsules-recall-deformed-or-melted-capsules. Based on FDA recall #D-1019-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1019-2018%22&limit=1).
Why it’s dangerous
The capsules may be deformed, clumped, or melted due to manufacturing issues. This could affect the medication's effectiveness and safety, but the recall does not indicate a risk of serious injury.
Who’s affected
Prescription patients who have the 50mg indomethacin capsules with NDC 31722-543-01. Those with specific medical conditions requiring this medication are most at risk.
How to tell if you have this one
Check for the product name 'Indomethacin Capsules, USP, 50 mg, 100-count bottles' with NDC 31722-543-01. These were manufactured for Camber Pharmaceuticals and sold in the US.
- Brand
Hetero Labs- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC code 31722-543-01 on the bottle label to confirm if you have the recalled product.
Questions people ask
Why is this product being recalled?
The recall is due to customer complaints of deformed, clumped, or melted capsules, which could affect the medication's effectiveness and safety.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact Hetero Labs directly for guidance.
Is this product safe to use?
The recall does not indicate a risk of serious injury, but the capsules may not be effective if deformed or melted.
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-1019-2018 — Hetero Labs Hetero Labs Hello, I own a Hetero Labs that is covered by recall D-1019-2018 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-1019-2018 (July 18, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1019-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.