Door County Coffee & Tea Co., Inc. Recall: Retail Box did not contain list of ingredients or allergen statement. - F-0271-2021
United States
TerminatedClass II
- Company
- Door County Coffee & Tea Co., Inc.
- Product
- Door County Coffee & Tea Co. French Vanilla Flavored Cappucc…
- Recall date
- January 21, 2021
- Terminated
- March 31, 2021
- Source
- FDA
Reason for recall
Retail Box did not contain list of ingredients or allergen statement.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. 10 Single Serve cups .51 oz (14g)/EA. Net Wt. 5.1 oz. (144g) | Not published in this source record | 3,325 boxes | Lot Code 1C092220-2 Expires 9/22/2022 Lot Code 1C120220-A Expires 12/2/2022. |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0271-2021
- Event ID
- 87206
- Status
- Terminated
- Classification
- Class II
- Company
- Door County Coffee & Tea Co., Inc.
- Product description
- Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. 10 Single Serve cups .51 oz (14g)/EA. Net Wt. 5.1 oz. (144g)
- Quantity
- 3,325 boxes
- Reason
- Retail Box did not contain list of ingredients or allergen statement.
- Recall initiation date
- January 21, 2021
- Report date
- February 10, 2021
- Classification date
- Not published in this source record
- Termination date
- March 31, 2021
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- Lot Code 1C092220-2 Expires 9/22/2022 Lot Code 1C120220-A Expires 12/2/2022.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Door County Coffee & Tea Co., 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. 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.
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?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of March 31, 2021.
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.