FDA Recall United States Terminated Historical recordClass I
The TJX Companies, Inc.
- Product
- Keats London Vegan Irish Cream Truffles in a 4.93-ounce rou…
- Published
- June 15, 2022
- Distribution
- Multiple states
The TJX Companies, Inc. Recall: Product contains undeclared sulfites at approx. 40 ppm.
United States
TerminatedClass II
- Company
- The TJX Companies, Inc.
- Product
- FUNKTIONAL FOODS brand SPIRULINA POWDER, NET WEIGHT 3.5 oz (…
- Recall date
- June 11, 2018
- Terminated
- July 10, 2018
- Source
- FDA
Reason for recall
Product contains undeclared sulfites at approx. 40 ppm.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| FUNKTIONAL FOODS brand SPIRULINA POWDER, NET WEIGHT 3.5 oz (100 g) with UPC Code: 060427570192 | Not published in this source record | 1200 units | UPC: 060427570192 Lot Code: F-704101 |
Distribution
- Distributed to TJX retail stored throughout the U.S. with 375 stored listed on the distribution list provided by firm.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1609-2018
- Event ID
- 80290
- Status
- Terminated
- Classification
- Class II
- Company
- The TJX Companies, Inc.
- Product description
- FUNKTIONAL FOODS brand SPIRULINA POWDER, NET WEIGHT 3.5 oz (100 g) with UPC Code: 060427570192
- Quantity
- 1200 units
- Reason
- Product contains undeclared sulfites at approx. 40 ppm.
- Recall initiation date
- June 11, 2018
- Report date
- July 11, 2018
- Classification date
- Not published in this source record
- Termination date
- July 10, 2018
- Distribution pattern
- Distributed to TJX retail stored throughout the U.S. with 375 stored listed on the distribution list provided by firm.
- UPC, lot, and code information
- UPC: 060427570192 Lot Code: F-704101
- 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: The TJX Companies, Inc.
Other recalls from The TJX Companies, 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
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- Product
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- Published
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- Distribution
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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.
