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RECALL RECORD — CLASS IRecall closedF-1675-2018/FDA enforcement
Ll's Magnetic Clay INC·Dietary Supplements·Jun 29, 2018

Prescript-assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary…

What you need to know

Class I

  • What happened

    The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Tree nuts such as almonds or walnuts were not declared, posing a risk to people with tree-nut allergy.

  • 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 nameLl's Magnetic Clay INC
Recalling firmLl's Magnetic Clay INCAustin, TX, United States
UPC / barcodes
8 53956 00315 78 53956 00353 9
Lot / date codes
  • All Lots within expiry
  • Lot # s: 1356300 (exp. 01/2019), 1405700 (exp. 03/2019), 17A128 (exp. 03/2021), W00103 (exp. 06/2019), 16A071, 17A130, 16C076, 15D081, W00095, 15K016, W0135, 15D007, 15D080, 16B174, 16A078, 16D065, 16B041, W0176, 15D115, 16A214.
Distribution area
Nationwide

Nationwide throughout the United States and United Kingdom, Mexico, Netherlands, Sweden, Australia, Canada, Hong Kong, Spain, New Zealand, Chile, Taiwan, Switzerland, Albania, Poland, Israel, Monaco, Japan, India, Hungary, Saudi Arabia, Malaysia, UAE, Norway, France, Russia, Australia, Colombia, Czech Republic, Nigeria, Ireland, Philippines

United States, Canada, Mexico, United Kingdom, Japan, Australia, France

Quantity affected290, 000 units
Recall initiationFDA report date: August 8, 2018
FDA recall numberF-1675-2018

Beyond the headline

The recall, in context

Ll's Magnetic Clay INC initiated this supplements recall on June 29, 2018. The FDA enforcement report states: The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts. The FDA report lists distribution as: Nationwide throughout the United States and United Kingdom, Mexico, Netherlands, Sweden, Australia, Canada, Hong Kong, Spain, New Zealand, Chile, Taiwan, Switzerland, Albania, Poland, Israel, Monaco, Japan, India, Hungary, Saudi Arabia, Malaysia, UAE, Norway, France, Russia, Australia, Colombia, Czech Republic, Nigeria, Ireland, Philippines.

The FDA enforcement report describes the reason as: The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.

Prescript-assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary… was made or distributed by Ll's Magnetic Clay INC in Austin, TX, United States. This page reflects FDA report F-1675-2018, dated August 8, 2018.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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

Undeclared tree nuts

Symptoms to watch for

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed tree-nut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a tree-nut allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Prescript-assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary… recall?

Ll's Magnetic Clay INC recalled Prescript-assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary… in an FDA Class I enforcement action reported as F-1675-2018. The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.

What are the symptoms of Undeclared tree nuts exposure?

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut allergy.

How quickly can Undeclared tree nuts symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared tree nuts?

People with a diagnosed tree-nut allergy, especially children and anyone with a history of anaphylaxis.

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. Do not eat the product if you have a tree-nut allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Ll's Magnetic Clay 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-1675-2018 and keep the packaging, lot code and proof of purchase if you have them.

Is the Ll's Magnetic Clay 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-1675-2018. 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.