FDA Recall United States Terminated Historical recordClass I
Rikki USA, Inc.
- Product
- Masas Gourmet Sweet and Sour Sauce, packaged in a glass jar…
- Published
- July 26, 2017
- Distribution
- distributed in CA, IL, NY, OR and WA.
Rikki USA, Inc. Recall: Hollandaise Sauce was recalled due to presence of mold.
United States
TerminatedClass III
- Company
- Rikki USA, Inc.
- Product
- Hollandaise Sauce, sold as Sallere Classic Sauces and Butter…
- Recall date
- October 5, 2016
- Terminated
- November 8, 2016
- Source
- FDA
Reason for recall
Hollandaise Sauce was recalled due to presence of mold.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Hollandaise Sauce, sold as Sallere Classic Sauces and Butters, refrigerated product. Each plastic tub has a net wt 7 oz. The label is read in parts: "***HOLLANDAISE SAUSE***Use on chicken, seafood and vegetables***. | Not published in this source record | 125 cases (or 750/7 oz. tubs total) | Lot # 1640288. Best by: 11-22-2016 |
Distribution
- distributed in MD and OR.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0377-2017
- Event ID
- 75390
- Status
- Terminated
- Classification
- Class III
- Company
- Rikki USA, Inc.
- Product description
- Hollandaise Sauce, sold as Sallere Classic Sauces and Butters, refrigerated product. Each plastic tub has a net wt 7 oz. The label is read in parts: "***HOLLANDAISE SAUSE***Use on chicken, seafood and vegetables***.
- Quantity
- 125 cases (or 750/7 oz. tubs total)
- Reason
- Hollandaise Sauce was recalled due to presence of mold.
- Recall initiation date
- October 5, 2016
- Report date
- November 9, 2016
- Classification date
- Not published in this source record
- Termination date
- November 8, 2016
- Distribution pattern
- distributed in MD and OR.
- UPC, lot, and code information
- Lot # 1640288. Best by: 11-22-2016
- 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
Responsible company: Rikki USA, Inc.
Other recalls from Rikki USA, Inc.
FDA Recall United States Terminated Historical recordClass I
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- Product
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- Published
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- Distribution
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FDA Recall United States Terminated Historical recordClass I
Rikki USA, Inc.
- Product
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- Published
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- Distribution
- distributed in CA, IL, NY, OR and WA.
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 |
|---|---|
| Maryland | 1 |
| Oregon | 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 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.
