FDA Recall United States Terminated Historical recordClass I
Gel Spice Co, Inc.
- Product
- Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) an…
- Published
- January 24, 2018
- Distribution
- The product was distributed thru out the…
Gel Spice Co, Inc. Recall: Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
United States
TerminatedClass I
- Company
- Gel Spice Co, Inc.
- Product
- Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) an…
- Recall date
- December 18, 2017
- Terminated
- June 29, 2018
- Source
- FDA
Reason for recall
Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count | Not published in this source record | 403 Cases | 1.7 oz (48 g) Best By Date Code(s). 11/20/20..... 3 1/2 oz Best By Date Code(s) 09/26/20, 11/06/20, 12/05/20 |
Distribution
- The product was distributed thru out the United States. AL
- AR
- CA
- CT
- FL
- GA
- PA
- OH
- NJ
- NY
- IA
- ID
- IL
- SC
- MD
- MT
- IN
- NH
- MI
- NC
- MN
- SD
- WA
- VA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0573-2018
- Event ID
- 78785
- Status
- Terminated
- Classification
- Class I
- Company
- Gel Spice Co, Inc.
- Product description
- Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count
- Quantity
- 403 Cases
- Reason
- Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
- Recall initiation date
- December 18, 2017
- Report date
- January 24, 2018
- Classification date
- Not published in this source record
- Termination date
- June 29, 2018
- Distribution pattern
- The product was distributed thru out the United States. AL, AR, CA, CT, FL, GA, PA, OH, NJ, NY,IA, ID, IL, SC, MD, MT, IN, NH, MI, NC, MN, SD, WA, VA,
- UPC, lot, and code information
- 1.7 oz (48 g) Best By Date Code(s). 11/20/20..... 3 1/2 oz Best By Date Code(s) 09/26/20, 11/06/20, 12/05/20
- 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 78785 with 1 other product entry in Public Health Trace.
Responsible company: Gel Spice Co, Inc.
Other recalls from Gel Spice Co, Inc.
FDA Recall United States Terminated Historical recordClass I
Gel Spice Co, Inc.
- Product
- Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) an…
- Published
- January 24, 2018
- Distribution
- The product was distributed thru out the…
FDA Recall United States Terminated Historical recordClass I
Gel Spice Co, Inc.
- Product
- 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by…
- Published
- March 22, 2017
- Distribution
- Nationwide
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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| California | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Pennsylvania | 1 |
| Ohio | 1 |
| New Jersey | 1 |
| New York | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| South Carolina | 1 |
| Maryland | 1 |
| Montana | 1 |
| Indiana | 1 |
| New Hampshire | 1 |
| Michigan | 1 |
| North Carolina | 1 |
| Minnesota | 1 |
| South Dakota | 1 |
| Washington | 1 |
| 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 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.
