Inner Health Group, Inc dba Michael's Naturopathic Programs Recall: May contain undeclared milk (in the form of calcium caseinate) and soy. - F-1869-2016
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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of December 16, 2016.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.