Black Rifle Coffee Company Recall: Possible plastic within final product packaging.
United States
TerminatedClass III
- Company
- Black Rifle Coffee Company
- Product
- Black Rifle Coffee Mac V Whole Bean Coffee 12oz PET bags 40…
- Recall date
- June 29, 2021
- Terminated
- December 17, 2021
- Source
- FDA
Reason for recall
Possible plastic within final product packaging.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Black Rifle Coffee Mac V Whole Bean Coffee 12oz PET bags 40 bags per case | Not published in this source record | 19,367 | Batch Numbers: 47112A, 47112B, 57112A Product Number: 30-111-12W Manufacturer Number: JP2 Best By Date: 06/23/22, 06/24/22 |
Distribution
- Tennessee
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0318-2022
- Event ID
- 89179
- Status
- Terminated
- Classification
- Class III
- Company
- Black Rifle Coffee Company
- Product description
- Black Rifle Coffee Mac V Whole Bean Coffee 12oz PET bags 40 bags per case
- Quantity
- 19,367
- Reason
- Possible plastic within final product packaging.
- Recall initiation date
- June 29, 2021
- Report date
- December 29, 2021
- Classification date
- Not published in this source record
- Termination date
- December 17, 2021
- Distribution pattern
- Tennessee
- UPC, lot, and code information
- Batch Numbers: 47112A, 47112B, 57112A Product Number: 30-111-12W Manufacturer Number: JP2 Best By Date: 06/23/22, 06/24/22
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Black Rifle Coffee Company
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
