FDA Recall United States TerminatedTerminated: June 21, 2017Historical recordClass II
Immune Tree, Inc (formerly ITG, Inc.)
- Product
- LeptiTrim6 Vanilla Shake Item No. 9907; 860 g. Brand Immune…
- Published
- September 28, 2016
- Distribution
- Nationwide
United States
TerminatedClass II
Immune Tree is recalling certain Immune Tree; Health Works; Immune Pro6; Good For You and Surthrival brand colostrum products due to undeclared milk allergen.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Colostrum6 Capsules 500mg, Item No 9901, 180 ct. Sold under the brands: Immune Tree, Immune Pro-6 (Not purchased since 8/25/2014), Surthrival, Good For You Canada. Packaged using HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle | Not published in this source record | Not published in this source record | Not published in this source record |
Responsible company: Immune Tree, Inc (formerly ITG, Inc.)
FDA Recall United States TerminatedTerminated: June 21, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: June 21, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: June 21, 2017Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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Retrieved by Public Health Trace:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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.
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This record is preserved as published by FDA, as of June 21, 2017.
Status as reported: Terminated.
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