Bell Plantation Inc. Recall: Analytical results for generic non-pathogenic E. coli surpassed firm's in-house specifications for finished product..
United States
TerminatedClass II
- Company
- Bell Plantation Inc.
- Product
- Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic…
- Recall date
- January 24, 2018
- Terminated
- May 23, 2018
- Source
- FDA
Reason for recall
Analytical results for generic non-pathogenic E. coli surpassed firm's in-house specifications for finished product..
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars | Not published in this source record | 6011 -16 oz. jars | Lot Code # 1117341169, Exp. 1/7/2020 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0868-2018
- Event ID
- 79057
- Status
- Terminated
- Classification
- Class II
- Company
- Bell Plantation Inc.
- Product description
- Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars
- Quantity
- 6011 -16 oz. jars
- Reason
- Analytical results for generic non-pathogenic E. coli surpassed firm's in-house specifications for finished product..
- Recall initiation date
- January 24, 2018
- Report date
- March 7, 2018
- Classification date
- Not published in this source record
- Termination date
- May 23, 2018
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- Lot Code # 1117341169, Exp. 1/7/2020
- 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: Bell Plantation Inc.
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.
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.
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