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RECALL RECORD — CLASS IIRecall closedF-1551-2013/FDA enforcement
Enzyme Formulations, INC.·Dietary Supplements·May 15, 2013

Enzyme Solutions, a Dietary Supplement, Formula 29, 8 OZ

What you need to know

Class II

  • What happened

    Enzymes Formulations Inc. is recalling Enzyme Solutions Formula 29 8 oz., lot 1225822 because of a labeling error at the manufacturing. This resulted in 10 jars incorrectly…

  • 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 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 FDAAL, AR, CA, CO +24 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameEnzyme Formulations, INC.
Recalling firmEnzyme Formulations, INC.Madison, WI, United States
UPC / barcodes
6 97706 04140 8
Lot / date codes
  • Lot 1225822
Distribution area
ALARCACOCTFLGAIAIDILINKYLAMAMIMONCNVNYOHPASCTXUTVAWAWIWV

AL, AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MI, MO, NC, NV, NY, OH, PA, SC, TX, UT, VA, WA, WI, WV.

United States

Quantity affected256 bottles
Recall initiationFDA report date: July 3, 2013
FDA recall numberF-1551-2013

Beyond the headline

The recall, in context

Enzyme Formulations, INC. initiated this supplements recall on May 15, 2013. The FDA enforcement report states: Enzymes Formulations Inc. is recalling Enzyme Solutions Formula 29 8 oz., lot 1225822 because of a labeling error at the manufacturing. This resulted in 10 jars incorrectly containing a Multiple Enzyme Powder. The FDA report lists distribution as: AL, AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MI, MO, NC,NV,NY, OH, PA, SC, TX, UT, VA, WA, WI, WV.

The FDA enforcement report describes the reason as: Enzymes Formulations Inc. is recalling Enzyme Solutions Formula 29 8 oz., lot 1225822 because of a labeling error at the manufacturing. This resulted in 10 jars incorrectly containing a Multiple Enzyme Powder.

Enzyme Solutions, a Dietary Supplement, Formula 29, 8 OZ was made or distributed by Enzyme Formulations, INC. in Madison, WI, United States. This page reflects FDA report F-1551-2013, dated July 3, 2013.

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

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code 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 Enzyme Solutions, a Dietary Supplement, Formula 29, 8 OZ recall?

Enzyme Formulations, INC. recalled Enzyme Solutions, a Dietary Supplement, Formula 29, 8 OZ in an FDA Class II enforcement action reported as F-1551-2013. Enzymes Formulations Inc. is recalling Enzyme Solutions Formula 29 8 oz., lot 1225822 because of a labeling error at the manufacturing. This resulted in 10 jars incorrectly…

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Enzyme Formulations, INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1551-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Enzyme Formulations, 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-1551-2013. 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

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