Lords Organics Llc Recall: Lord Organics is recalling ginger powder because it has the potential to be contaminated with Salmonella.
United States
TerminatedClass I
- Company
- Lords Organics Llc
- Product
- Organic Veda brand Ginger Powder, 24 jars, Net Wt. 16 oz. (4…
- Recall date
- April 27, 2017
- Terminated
- August 31, 2017
- Source
- FDA
Reason for recall
Lord Organics is recalling ginger powder because it has the potential to be contaminated with Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Organic Veda brand Ginger Powder, 24 jars, Net Wt. 16 oz. (454 grams) | Not published in this source record | 96 units | Batch No: A324DGRP, MFD: AUG 2015, Best before: July 2017 |
Distribution
- US: Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2236-2017
- Event ID
- 77151
- Status
- Terminated
- Classification
- Class I
- Company
- Lords Organics Llc
- Product description
- Organic Veda brand Ginger Powder, 24 jars, Net Wt. 16 oz. (454 grams)
- Quantity
- 96 units
- Reason
- Lord Organics is recalling ginger powder because it has the potential to be contaminated with Salmonella.
- Recall initiation date
- April 27, 2017
- Report date
- May 31, 2017
- Classification date
- Not published in this source record
- Termination date
- August 31, 2017
- Distribution pattern
- US: Nationwide
- UPC, lot, and code information
- Batch No: A324DGRP, MFD: AUG 2015, Best before: July 2017
- 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: Lords Organics Llc
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.
