Food Recall Check
Class I · High risk Terminated Initiated Jun 29, 2018 (8 years ago)

Prescript-Assist Broad Spectrum Probiotic & Prebiotic… recall

Recalled by Ll's Magnetic Clay INC · Austin, TX, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Undeclared allergens: Milk Egg Peanut Tree nuts Shellfish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 290,000 units

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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 it was sold

Nationwide.

FDA's distribution note: 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

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, egg, peanut, tree nuts, shellfish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Ll's Magnetic Clay INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 29, 2018
In FDA report of
Aug 8, 2018
Terminated
Feb 8, 2019
FDA recall number
F-1675-2018 · event 80419
Official record
FDA enforcement report search

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