FDA Recall United States Terminated Historical recordClass II
Ajinomoto Windsor Inc., Golden Tiger Plant
- Product
- Molly's Kitchen Battered Green Beans, 6/2 lb. bags., Product…
- Published
- September 28, 2016
- Distribution
- U.S.
Ajinomoto Windsor Inc., Golden Tiger Plant Recall: Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated with E. coli O121.
United States
TerminatedClass II
- Company
- Ajinomoto Windsor Inc., Golden Tiger Plant
- Product
- Molly's Kitchen Hotzzarella Cheese Sticks, 12 lbs., Item No.…
- Recall date
- July 14, 2016
- Terminated
- February 16, 2017
- Source
- FDA
Reason for recall
Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated with E. coli O121.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Molly's Kitchen Hotzzarella Cheese Sticks, 12 lbs., Item No. 582648; Fred's Hotzzarella Cheese Sticks, 12lbs., Item No. 0204320. | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- US: AR
- AZ
- CA
- CT
- FL
- GA
- IA
- ID
- IL
- IN
- KS
- MA
- MI
- MN
- MO
- MT
- MX
- NE
- NV
- NY
- OH
- OR
- PA
- TN
- TX
- WA
- WI
- WV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2275-2016
- Status
- Terminated
- Classification
- Class II
- Company
- Ajinomoto Windsor Inc., Golden Tiger Plant
- Product description
- Molly's Kitchen Hotzzarella Cheese Sticks, 12 lbs., Item No. 582648; Fred's Hotzzarella Cheese Sticks, 12lbs., Item No. 0204320.
- Quantity
- Not published in this source record
- Reason
- Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated with E. coli O121.
- Recall initiation date
- July 14, 2016
- Report date
- September 21, 2016
- Classification date
- Not published in this source record
- Termination date
- February 16, 2017
- Distribution pattern
- US: AR, AZ, CA, CT, FL, GA, IA, ID, IL, IN, KS, MA, MI, MN, MO, MT, MX, NE, NV, NY, OH, OR, PA, TN, TX, WA, WI, WV
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Ajinomoto Windsor Inc., Golden Tiger Plant
Other recalls from Ajinomoto Windsor Inc., Golden Tiger Plant
FDA Recall United States Terminated Historical recordClass II
Ajinomoto Windsor Inc., Golden Tiger Plant
- Product
- 1. AJINOMOTO VEGETABLE FRIED RICE, Net Wt. 27 lb (9 ct./3 l…
- Published
- September 28, 2016
- Distribution
- U.S.
FDA Recall United States Terminated Historical recordClass II
Ajinomoto Windsor Inc., Golden Tiger Plant
- Product
- VIP-STEAMWORKS MIX VEGETABLES, 12 pk./12 oz., Product # 7007…
- Published
- September 28, 2016
- Distribution
- U.S.
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 |
|---|---|
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Massachusetts | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| Nebraska | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| West Virginia | 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.
