FDA Recall United States Terminated Historical recordClass II
Vitamin Cottage Natural Food Markets, Inc.
- Product
- NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO, 8 oz.…
- Published
- April 8, 2020
- Distribution
- Multiple states
Vitamin Cottage Natural Food Markets, Inc. Recall: Undeclared peanut and milk allergens
United States
TerminatedClass II
- Company
- Vitamin Cottage Natural Food Markets, Inc.
- Product
- NATURAL GROCERS ALMOND CLUSTERS DK CHOCOLATE NON-GMO, 8 oz.…
- Recall date
- February 19, 2020
- Terminated
- December 11, 2020
- Source
- FDA
Reason for recall
Undeclared peanut and milk allergens
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| NATURAL GROCERS ALMOND CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087236088, Packaged by Vitamin Cottage Natural Food Markets, Inc., Lakewood, CO 80228 | 000087236088 | 17,041 - 8 ox bags | Product number (ASP): 789977, PLU: 7236, Packed On: All Pack Dates 19-190 thru 20-048. |
Distribution
- AR
- AZ
- CO
- IA
- ID
- KS
- LA
- MN
- MO
- MT
- NE
- NV
- NM
- ND
- OK
- OR
- TX
- UT
- WA
- WY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0877-2020
- Event ID
- 85023
- Status
- Terminated
- Classification
- Class II
- Company
- Vitamin Cottage Natural Food Markets, Inc.
- Product description
- NATURAL GROCERS ALMOND CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087236088, Packaged by Vitamin Cottage Natural Food Markets, Inc., Lakewood, CO 80228
- Quantity
- 17,041 - 8 ox bags
- Reason
- Undeclared peanut and milk allergens
- Recall initiation date
- February 19, 2020
- Report date
- April 8, 2020
- Classification date
- Not published in this source record
- Termination date
- December 11, 2020
- Distribution pattern
- AR, AZ, CO, IA, ID, KS, LA, MN, MO, MT, NE, NV, NM, ND, OK, OR, TX, UT, WA, WY
- UPC, lot, and code information
- UPC 000087236088; Product number (ASP): 789977, PLU: 7236, Packed On: All Pack Dates 19-190 thru 20-048.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 85023 with 1 other product entry in Public Health Trace.
Responsible company: Vitamin Cottage Natural Food Markets, Inc.
Other recalls from Vitamin Cottage Natural Food Markets, Inc.
FDA Recall United States Terminated Historical recordClass II
Vitamin Cottage Natural Food Markets, Inc.
- Product
- Amaranth Grain Organic, brand Natural Grocers, packaged in p…
- Published
- August 10, 2022
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Vitamin Cottage Natural Food Markets, Inc.
- Product
- NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO, 8 oz.…
- Published
- April 8, 2020
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Vitamin Cottage Natural Food Markets, Inc.
- Product
- Natural Grocers Organic Extra Virgin Coconut Oil, packaged i…
- Published
- March 11, 2020
- Distribution
- 157 Natural Grocers' stores in AR, AZ, C…
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 |
|---|---|
| Arkansas | 1 |
| Arizona | 1 |
| Colorado | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Kansas | 1 |
| Louisiana | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| Nebraska | 1 |
| Nevada | 1 |
| New Mexico | 1 |
| North Dakota | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Texas | 1 |
| Utah | 1 |
| Washington | 1 |
| Wyoming | 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.
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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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.
