United States
TerminatedClass I
Produces contains undeclared milk.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Back to Nature, Gluten Free, Dark Chocolate Coconut Granola, 11 oz (311g) pouches, 6 pouches per case. UPC 8-19898-01225-8. | 8-19898-01225-8 | 5,448 cases (32,688 pouches) | Lot Codes/ Exp Date (Production Date): 9 MAY 17 (9 JUL 16), 10 MAY 17 (10 JUL 16), 11 MAY 17 (11 JUL 16), 13 JUN 17 (13 AUG 16), 14 JUN 17 (14 AUG 16). |
This recall shares FDA event ID 75585 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: August 31, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: August 31, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: August 31, 2017Historical recordClass I
Responsible company: Back To Nature Foods, Llc
FDA Recall United States TerminatedTerminated: August 31, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: August 31, 2017Historical recordClass I
FDA Recall United States TerminatedTerminated: August 31, 2017Historical recordClass I
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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 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.
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class I. 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.
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
This record is preserved as published by FDA, as of August 31, 2017.
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.
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