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Class I: serious health riskTerminated

Ll'S Magnetic Clay Prescript-Assist Broad Spectrum Probiotic & Recall

Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary…

LL'S MAGNETIC CLAY INC · Austin, TX

Risk level
Class I
Reported by FDA
Aug 8, 2018
Recall ID
F-1675-2018
Check your lot numberHow we source this data

Summary

Ll'S Magnetic Clay recalled Prescript-Assist Broad Spectrum Probiotic & starting Jun 29, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-1675-2018 on Aug 8, 2018. Reason: The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts. Status: Terminated.

Why it was recalled

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

Product description

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

Lot numbers, UPCs & expiration codes

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 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 to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1675-2018
Classification
Class I
Status
Terminated
Recall initiated
Jun 29, 2018
FDA report date
Aug 8, 2018
Quantity
290,000 units
Recall type
Voluntary: Firm initiated
Recalling firm
LL'S MAGNETIC CLAY INC

Original FDA data

Every field from FDA enforcement report F-1675-2018, exactly as published.

Show all FDA fields
City
Austin
State
TX
Status
Terminated
Country
United States
Event ID
80419
Address
2301 Scarbrough Dr
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.
Postal code
78728-4748
Report date
Aug 8, 2018
Product type
Food
Recall number
F-1675-2018
Classification
Class I
Recalling firm
LL'S MAGNETIC CLAY INC
Product quantity
290,000 units
Termination date
Feb 8, 2019
Reason for recall
The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
Distribution pattern
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
Recall initiation date
Jun 29, 2018
Initial firm notification
Press Release
Center classification date
Jul 30, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1675-2018, published Aug 8, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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