FDA Recall United States Terminated Historical recordClass II
Midwest International Corp
- Product
- LONGAN ARIL, Net Wt: 7.4oz (210g), contains yellow and orang…
- Published
- January 11, 2017
- Distribution
- IL, MA, TX thru 5 retail stores
Midwest International Corp Recall: The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does not declare saccharin on it's labeling and the the product appears to contain or bear the following unsafe color additive such as FD&C Yellow #5 (C.I. No. 19140 - tartrazine) FD&C Red #3 (C.I. No. 45430 - Erythrosine), and Carmoisine (C.I. No. 14720 - former ext. D&C Red #10).
United States
TerminatedClass II
- Company
- Midwest International Corp
- Product
- LONGAN ARIL, NET WT: 10.6oz (300g), contains blue labeling
- Recall date
- November 23, 2016
- Terminated
- June 20, 2018
- Source
- FDA
Reason for recall
The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does not declare saccharin on it's labeling and the the product appears to contain or bear the following unsafe color additive such as FD&C Yellow #5 (C.I. No. 19140 - tartrazine) FD&C Red #3 (C.I. No. 45430 - Erythrosine), and Carmoisine (C.I. No. 14720 - former ext. D&C Red #10).
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| LONGAN ARIL, NET WT: 10.6oz (300g), contains blue labeling | Not published in this source record | 39 cartons/30 units | none |
Distribution
- IL
- MA
- TX thru 5 retail stores
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1162-2017
- Event ID
- 75808
- Status
- Terminated
- Classification
- Class II
- Company
- Midwest International Corp
- Product description
- LONGAN ARIL, NET WT: 10.6oz (300g), contains blue labeling
- Quantity
- 39 cartons/30 units
- Reason
- The item is subject to Import Alert 21-04 in that it appears to bear or contain cyclamate and dulcin which are unsafe food additives, the item does not declare saccharin on it's labeling and the the product appears to contain or bear the following unsafe color additive such as FD&C Yellow #5 (C.I. No. 19140 - tartrazine) FD&C Red #3 (C.I. No. 45430 - Erythrosine), and Carmoisine (C.I. No. 14720 - former ext. D&C Red #10).
- Recall initiation date
- November 23, 2016
- Report date
- January 11, 2017
- Classification date
- Not published in this source record
- Termination date
- June 20, 2018
- Distribution pattern
- IL, MA, TX thru 5 retail stores
- UPC, lot, and code information
- none
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- 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 75808 with 1 other product entry in Public Health Trace.
Responsible company: Midwest International Corp
Other recalls from Midwest International Corp
FDA Recall United States Terminated Historical recordClass II
Midwest International Corp
- Product
- LONGAN ARIL, Net Wt: 7.4oz (210g), contains yellow and orang…
- Published
- January 11, 2017
- Distribution
- IL, MA, TX thru 5 retail stores
FDA Recall United States Terminated Historical recordClass II
Midwest International Corp
- Product
- DRIED VEGETABLE, NET WT: 17.6oz (500g)
- Published
- December 28, 2016
- Distribution
- MA, IL, & TX thru 4 retail stores
FDA Recall United States Terminated Historical recordClass II
Midwest International Corp
- Product
- Malayuguo, USA jiazhoufengwei, Fish, NET WT 4.2oz (120g)
- Published
- December 28, 2016
- Distribution
- CA, IL, NY, MD, MA, KY, TX and VA
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 |
|---|---|
| Illinois | 1 |
| Massachusetts | 1 |
| Texas | 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.
