Inner Health Group, Inc dba Michael's Naturopathic Programs Recall: May contain undeclared milk (in the form of calcium caseinate) and soy.
United States
TerminatedClass I
- Company
- Inner Health Group, Inc dba Michael's Naturopathic Programs
- Product
- Michael's Naturopathic Programs Cholesterol Metabolism Facto…
- Recall date
- June 23, 2016
- Terminated
- December 16, 2016
- Source
- FDA
Reason for recall
May contain undeclared milk (in the form of calcium caseinate) and soy.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Michael's Naturopathic Programs Cholesterol Metabolism Factors 270 count, 180 count, and 90 count tablets packaged in plastic bottles | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1869-2016
- Status
- Terminated
- Classification
- Class I
- Company
- Inner Health Group, Inc dba Michael's Naturopathic Programs
- Product description
- Michael's Naturopathic Programs Cholesterol Metabolism Factors 270 count, 180 count, and 90 count tablets packaged in plastic bottles
- Quantity
- Not published in this source record
- Reason
- May contain undeclared milk (in the form of calcium caseinate) and soy.
- Recall initiation date
- June 23, 2016
- Report date
- August 10, 2016
- Classification date
- Not published in this source record
- Termination date
- December 16, 2016
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Inner Health Group, Inc dba Michael's Naturopathic Programs
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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