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RECALL RECORD — CLASS IIRecall closedF-0705-2020/FDA enforcement
Abh Nature's Products, INC.·Dietary Supplements·Jan 21, 2020

All Dietary Supplement Manufactured and Distributed by Abh Nature's Products INC

What you need to know

Class II

  • What happened

    Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Current good manufacturing practice failures can affect product identity, strength, quality or purity.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameAbh Nature's Products, INC.
Recalling firmAbh Nature's Products, INC.Edgewood, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • To be determined
Distribution area
Nationwide

Nationwide and Worldwide

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: February 26, 2020
FDA recall numberF-0705-2020

Beyond the headline

The recall, in context

Abh Nature's Products, INC. initiated this supplements recall on January 21, 2020. The FDA enforcement report states: Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP). The FDA report lists distribution as: Nationwide and Worldwide.

The FDA enforcement report describes the reason as: Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).

All Dietary Supplement Manufactured and Distributed by Abh Nature's Products INC was made or distributed by Abh Nature's Products, INC. in Edgewood, NY, United States. This page reflects FDA report F-0705-2020, dated February 26, 2020.

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, current good manufacturing practice failures can affect product identity, strength, quality or purity.

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

    Do not eat, drink or take the affected product.

  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 All Dietary Supplement Manufactured and Distributed by Abh Nature's Products INC recall?

Abh Nature's Products, INC. recalled All Dietary Supplement Manufactured and Distributed by Abh Nature's Products INC in an FDA Class II enforcement action reported as F-0705-2020. Firm ordered by consent decree to recall all products because the products were prepared, packed, or held in violation of current good manufacturing practice regulation (cGMP).

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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 Abh Nature's Products, 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-0705-2020. 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.