RECALL RECORD — CLASS IIRecall closedF-0321-2015/FDA enforcement

Kidney & Bladder Foundation, 4 OZ Bottle, 550 Oliver Dr Troy, Mi 48084 the Quality Herb That…

What you need to know

Class II
  • What happened

    Products not manufactured under GMP's

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall closed · classified by the FDAAZ, CA, CT, FL +14 moreMore cosmetics

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Product identification

Source: FDA FOOD

Brand nameGood Herbs, INC.
Recalling firmGood Herbs, INC.Troy, MI, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • All Lots distributed on or after October 17, 2013
Distribution area
AZCACTFLINMEMIMOMSNCNHNYOHORRITXVAWY

National: AZ, CA, CT, FL, IN, ME, MI, MO, MS, NC, NH, NY, OH, OR, RI, TX, VA & WY International: None reported

United States

Quantity affectedApproximately 901 total units for all products
Recall initiationFDA report date: November 5, 2014
FDA recall numberF-0321-2015

Beyond the headline

The recall, in context

Good Herbs, INC. initiated this cosmetics recall on May 5, 2014. The FDA enforcement report states: Products not manufactured under GMP's. The FDA report lists distribution as: National: AZ, CA, CT, FL, IN, ME, MI, MO, MS, NC, NH, NY, OH, OR, RI, TX, VA & WY International: None reported.

The FDA enforcement report describes the reason as: Products not manufactured under GMP's

Kidney & Bladder Foundation, 4 OZ Bottle, 550 Oliver Dr Troy, Mi 48084 the Quality Herb That… was made or distributed by Good Herbs, INC. in Troy, MI, United States. This page reflects FDA report F-0321-2015, dated November 5, 2014.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Kidney & Bladder Foundation, 4 OZ Bottle, 550 Oliver Dr Troy, Mi 48084 the Quality Herb That… recall?

Good Herbs, INC. recalled Kidney & Bladder Foundation, 4 OZ Bottle, 550 Oliver Dr Troy, Mi 48084 the Quality Herb That… in an FDA Class II enforcement action reported as F-0321-2015. Products not manufactured under GMP's

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Good Herbs, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0321-2015. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.