LL'S MAGNETIC CLAY product recalled over undeclared allergens
- Recall date
- June 29, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- LL'S MAGNETIC CLAY INC recalls Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-cap…
- Recall number
- F-1675-2018
- FDA classification
- Class I
- Brand / firm
- LL'S MAGNETIC CLAY INC
- Sold / 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, Cz…
Why it was recalled
The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
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