The Recall Desk
Agency classClass IOur severity:CriticalFDA (Food)·F-1675-2018·Announced 2018-08-08

Probiotic Supplement Recalled for Potential Undeclared Allergens

LL'S Magnetic Clay Inc. is recalling Prescript-Assist Probiotic & Prebiotic supplements because they may contain undeclared almonds, shellfish, milk, eggs, or peanuts.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The FDA has classified this recall as Class I, which indicates a reasonable probability that the use of, or exposure to, the violative product will cause serious adverse health consequences or death, particularly for individuals with severe allergies.

Plain-English summary

LL'S Magnetic Clay Inc. is voluntarily recalling Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement. The recall involves 60-capsule and 90-capsule bottles distributed nationwide in the United States and in numerous international markets, including the United Kingdom, Canada, and Australia.

The FDA has classified this as a Class I recall because the product has the potential to contain undeclared allergens, specifically almonds, shellfish, milk, eggs, and peanuts. The recall covers approximately 290,000 units across multiple lot numbers, all of which are within their expiration dates.

Consumers who have purchased this product should stop using it immediately. Individuals with allergies to any of the listed ingredients should be particularly cautious. Consumers can contact the recalling firm for further information or to arrange a refund.

The recalled product

Product
Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
Affected units
290,000

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • 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

Distribution

Distributed nationwide across the United States.

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