FDA Recall United States Terminated Historical recordClass II
Tradewind Foods de Puerto Rico Inc.
- Product
- Goya Red Kidney Beans, Net Wt.15.5oz.(439g), metal (tin) can…
- Published
- May 15, 2024
- Distribution
- The product was distributed only in Puer…
Tradewind Foods de Puerto Rico Inc. Recall: Goya Honey with Comb product tested by FDA showed presence of 2, 6 Dichlorobenzamide which is not EPA registered for use in honey.
United States
TerminatedClass III
- Company
- Tradewind Foods de Puerto Rico Inc.
- Product
- Label reads in part as " GOYA ***HONEY WITH COMB***PURE ALL…
- Recall date
- June 7, 2016
- Terminated
- May 30, 2017
- Source
- FDA
Reason for recall
Goya Honey with Comb product tested by FDA showed presence of 2, 6 Dichlorobenzamide which is not EPA registered for use in honey.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Label reads in part as " GOYA ***HONEY WITH COMB***PURE ALL NATURAL***NET WT. 16 OZ (1LB)***15173***GOYA FOODS, INC. SECAUCUS, NJ 07096" | Not published in this source record | 297 cases/12 jars per case | 15173 |
Distribution
- Domestic: Puerto Rico and US Virgin Islands (St. Croix and St. John); International: St. Marteen
- Anguila
- Tortola
- Curacao
- and Aruba.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2602-2016
- Event ID
- 74327
- Status
- Terminated
- Classification
- Class III
- Company
- Tradewind Foods de Puerto Rico Inc.
- Product description
- Label reads in part as " GOYA ***HONEY WITH COMB***PURE ALL NATURAL***NET WT. 16 OZ (1LB)***15173***GOYA FOODS, INC. SECAUCUS, NJ 07096"
- Quantity
- 297 cases/12 jars per case
- Reason
- Goya Honey with Comb product tested by FDA showed presence of 2, 6 Dichlorobenzamide which is not EPA registered for use in honey.
- Recall initiation date
- June 7, 2016
- Report date
- October 5, 2016
- Classification date
- Not published in this source record
- Termination date
- May 30, 2017
- Distribution pattern
- Domestic: Puerto Rico and US Virgin Islands (St. Croix and St. John); International: St. Marteen, Anguila, Tortola, Curacao, and Aruba.
- UPC, lot, and code information
- 15173
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Tradewind Foods de Puerto Rico Inc.
Other recalls from Tradewind Foods de Puerto Rico Inc.
FDA Recall United States Terminated Historical recordClass I
Tradewind Foods de Puerto Rico Inc.
- Product
- GOYA Adobo, All Purpose Seasoning with Cumin, Goya Foods, In…
- Published
- December 13, 2017
- Distribution
- P.R. consignees only.
FDA Recall United States Terminated Historical recordClass I
Tradewind Foods de Puerto Rico Inc.
- Product
- GOYA Adobo, All Purpose Seasoning with Pepper, Goya Foods, I…
- Published
- December 13, 2017
- Distribution
- P.R. consignees only.
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
