Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary…
Recalling firm: LL'S MAGNETIC CLAY INC
The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 8, 2019.
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FDA code information
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.
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Full FDA record and distribution details
Original product description
Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
Original FDA recall reason
The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
Recall details
- Recall number
- F-1675-2018
- Event ID
- 80419
- FDA status
- Terminated
- Initiated
- Jun 29, 2018
- Reported
- Aug 8, 2018
- Classified
- Jul 30, 2018
- Terminated
- Feb 8, 2019
- Quantity
- 290,000 units
- Location
- Austin, TX, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
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
Data updated September 16, 2026. View official FDA data ↗
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