FDA Recall United States Terminated Historical recordClass I
American Instants, Inc.
- Product
- Spicy Chai Latte 50 lb. box
- Published
- January 25, 2017
- Distribution
- CA, FL, IL, OH PA, NJ & NY; Foreign
American Instants, Inc. Recall: America Instant Inc. is recalling various chai tea products due to buttermilk and milk products that may be contaminated with Salmonella and were provided by another supplier.
United States
TerminatedClass I
- Company
- American Instants, Inc.
- Product
- Cappucino Supreme Gourmet Chai Net Wt. 2 lbs.
- Recall date
- December 8, 2016
- Terminated
- May 1, 2018
- Source
- FDA
Reason for recall
America Instant Inc. is recalling various chai tea products due to buttermilk and milk products that may be contaminated with Salmonella and were provided by another supplier.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Cappucino Supreme Gourmet Chai Net Wt. 2 lbs. | Not published in this source record | 2232 lbs. | lot# 3026F |
Distribution
- CA
- FL
- IL
- OH PA
- NJ & NY; Foreign
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1279-2017
- Event ID
- 75935
- Status
- Terminated
- Classification
- Class I
- Company
- American Instants, Inc.
- Product description
- Cappucino Supreme Gourmet Chai Net Wt. 2 lbs.
- Quantity
- 2232 lbs.
- Reason
- America Instant Inc. is recalling various chai tea products due to buttermilk and milk products that may be contaminated with Salmonella and were provided by another supplier.
- Recall initiation date
- December 8, 2016
- Report date
- January 25, 2017
- Classification date
- Not published in this source record
- Termination date
- May 1, 2018
- Distribution pattern
- CA, FL, IL, OH PA, NJ & NY; Foreign
- UPC, lot, and code information
- lot# 3026F
- 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
Other products recalled under this same event
This recall shares FDA event ID 75935 with 3 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
American Instants, Inc.
- Product
- Colonial International Chai Latte Net Wt. 2 lbs.
- Published
- January 25, 2017
- Distribution
- CA, FL, IL, OH PA, NJ & NY; Foreign
FDA Recall United States Terminated Historical recordClass I
American Instants, Inc.
- Product
- Sun Caf¿ (D Blend) Spice Chai Net Wt. 2 lbs. Made in USA…
- Published
- January 25, 2017
- Distribution
- CA, FL, IL, OH PA, NJ & NY; Foreign
Responsible company: American Instants, Inc.
Other recalls from American Instants, Inc.
FDA Recall United States Terminated Historical recordClass I
American Instants, Inc.
- Product
- Spicy Chai Latte 50 lb. box
- Published
- January 25, 2017
- Distribution
- CA, FL, IL, OH PA, NJ & NY; Foreign
FDA Recall United States Terminated Historical recordClass I
American Instants, Inc.
- Product
- Colonial International Chai Latte Net Wt. 2 lbs.
- Published
- January 25, 2017
- Distribution
- CA, FL, IL, OH PA, NJ & NY; Foreign
FDA Recall United States Terminated Historical recordClass I
American Instants, Inc.
- Product
- Sun Caf¿ (D Blend) Spice Chai Net Wt. 2 lbs. Made in USA…
- Published
- January 25, 2017
- Distribution
- CA, FL, IL, OH PA, NJ & NY; Foreign
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 |
|---|---|
| California | 1 |
| Florida | 1 |
| Illinois | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| New Jersey | 1 |
| New York | 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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
