Good Herbs DI-ZYME Capsules Recall: Not Manufactured Under GMPs

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Recalling firmGood Herbs, Inc.550 Oliver Dr, N/A · Troy, MI 48084-5468

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Good Herbs Inc. is recalling DI-ZYME capsules produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could affect product safety and quality.

Why it’s dangerous

The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This could mean the product might not meet expected safety and quality standards, but does not indicate an immediate risk of injury or illness.

Who’s affected

People who bought DI-ZYME capsules from Good Herbs Inc. between October 17, 2013 and present. Those with health conditions requiring herbal supplements may be at slightly higher risk.

How to tell if you have this one

Check the product label for the manufacturer's address: 550 Oliver Dr Troy, MI 48084. Look for the production date on or after October 17, 2013.

Brand
Good Herbs
Category
Food

Based on the official FDA remedy

What to do — step by step

Check Product Date
Look for the production date on the capsule label, which should be on or after October 17, 2013.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality.

How can I tell if I have the recalled product?

Check the product label for the manufacturer's address: 550 Oliver Dr Troy, MI 48084 and the production date on or after October 17, 2013.

What should I do if I have the recalled product?

The recall record does not specify a remedy, so you may want to contact Good Herbs Inc. for further guidance.

Take action

Contact Good Herbs

We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall F-0175-2015 — Good Herbs Good Herbs

Hello,

I own a Good Herbs that is covered by recall F-0175-2015 from Good Herbs.

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 #F-0175-2015 (March 25, 2014) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0175-2015 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Good Herbs, Inc. recalls Good Herbs, Inc., DI-ZYME, capsules, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works

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