FDA Recall United States Terminated Historical recordClass I
Hormel Foods Corporation
- Product
- PLANTERS¿ Honey Roasted Peanuts 4oz UPC 2900002097. Package…
- Published
- June 12, 2024
- Distribution
- Distributed to distribution centers in…
Hormel Foods Corporation Recall: Aflatoxin level slightly above actionable limit
United States
TerminatedClass II
- Company
- Hormel Foods Corporation
- Product
- SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723…
- Recall date
- September 28, 2020
- Terminated
- December 2, 2020
- Source
- FDA
Reason for recall
Aflatoxin level slightly above actionable limit
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container | 00037600110723 | 15,352 cases = 184,224 jars | Lot # BEST IF USED BY SEP2921 LR3 |
Distribution
- AL
- AR
- CA
- CO
- CT
- DE
- FL
- GA
- IA
- ID
- IL
- IN
- KS
- KY
- MA
- MD
- ME
- MI
- MN
- MO
- NC
- NH
- NJ
- NY
- OH
- OR
- PA
- RI
- SC
- TN
- UT
- VA
- VT
- WA
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0030-2021
- Event ID
- 86514
- Status
- Terminated
- Classification
- Class II
- Company
- Hormel Foods Corporation
- Product description
- SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container
- Quantity
- 15,352 cases = 184,224 jars
- Reason
- Aflatoxin level slightly above actionable limit
- Recall initiation date
- September 28, 2020
- Report date
- October 14, 2020
- Classification date
- Not published in this source record
- Termination date
- December 2, 2020
- Distribution pattern
- AL, AR, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NH, NJ, NY, OH, OR, PA, RI, SC, TN, UT, VA, VT, WA, WI
- UPC, lot, and code information
- UPC 00037600110723; Lot # BEST IF USED BY SEP2921 LR3
- 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
Responsible company: Hormel Foods Corporation
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FDA Recall United States Terminated Historical recordClass II
Hormel Foods Corporation
- Product
- Great Shake Plus Fortified Nutrition, Soy Formula, Strawberr…
- Published
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- Distribution
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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 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Utah | 1 |
| Virginia | 1 |
| Vermont | 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.
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.
