CLASS I Food recall · Reported 8 Aug 2018 · FDA Enforcement Report

Prescript-Assist Broad Spectrum Probiotic & Prebiotic recalled

Ll's Magnetic Clay is recalling Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary, distributed nationwide in the US. The recall was initiated on 29 Jun 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll 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.
Quantity recalled290,000 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1675-2018
FDA event ID
80419
Recalling firm
Ll's Magnetic Clay, Austin, TX
Classification
Class I
Status
Terminated
Recall initiated
29 Jun 2018
FDA classified
30 Jul 2018
Reported
8 Aug 2018
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Allergens
Product category
Probiotics

Timeline

29 Jun 2018Recall initiated by company
30 Jul 2018Classified by FDA+31 days
8 Aug 2018Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539

Where it was distributed

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

Nationwide

Questions about this recall

Is Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary recalled?

Yes. Ll's Magnetic Clay recalled Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary on 29 Jun 2018. The recall is Class I and its status is Terminated. Recall number F-1675-2018.

Why was it recalled?

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

Which lots are affected?

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.

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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