FDA Recall United States TerminatedTerminated: May 28, 2021Historical recordClass I
Pure Ground Ingredients
- Product
- Pure Ground Ingredients Organic Fennel Seed, Ground 35 lb.…
- Published
- July 24, 2019
- Distribution
- Multiple states
Pure Ground Ingredients Recall: Product tested and found to be positive for Salmonella - F-1560-2019
United States
TerminatedClass I
- Company
- Pure Ground Ingredients
- Product
- Pure Ground Ingredients Organic Fennel Seed, Tea bag Cut 4…
- Recall date
- June 28, 2019
- Terminated
- May 28, 2021
- Source
- FDA
Reason for recall
Product tested and found to be positive for Salmonella
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pure Ground Ingredients Organic Fennel Seed, Tea bag Cut 40 lb. bags; Item # FENO-TC Processed and Packaged by: Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423 | Not published in this source record | 1820 lbs. total - both cuts | Incoming lot 01-465; FENO-5041847Z-TC-126F (tea cut) Expiration Date: June 2021 |
Distribution
- CA
- NC
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1560-2019
- Event ID
- 83244
- Status
- Terminated
- Classification
- Class I
- Company
- Pure Ground Ingredients
- Product description
- Pure Ground Ingredients Organic Fennel Seed, Tea bag Cut 40 lb. bags; Item # FENO-TC Processed and Packaged by: Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423
- Quantity
- 1820 lbs. total - both cuts
- Reason
- Product tested and found to be positive for Salmonella
- Recall initiation date
- June 28, 2019
- Report date
- July 24, 2019
- Classification date
- Not published in this source record
- Termination date
- May 28, 2021
- Distribution pattern
- CA, NC, WI
- UPC, lot, and code information
- Incoming lot 01-465; FENO-5041847Z-TC-126F (tea cut) Expiration Date: June 2021
- 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
Other products recalled under this same event
This recall shares FDA event ID 83244 with 1 other product entry in Public Health Trace.
Responsible company: Pure Ground Ingredients
Other recalls from Pure Ground Ingredients
FDA Recall United States TerminatedTerminated: August 16, 2024Historical recordClass I
Pure Ground Ingredients
- Product
- Pure Ground Ingredients Organic Oregano Leaf Powder Item#: O…
- Published
- July 13, 2022
- Distribution
- U.S. distribution to the following: OR,…
FDA Recall United States TerminatedTerminated: May 28, 2021Historical recordClass I
Pure Ground Ingredients
- Product
- Pure Ground Ingredients Organic Fennel Seed, Ground 35 lb.…
- Published
- July 24, 2019
- Distribution
- Multiple states
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 |
|---|---|
| California | 1 |
| North Carolina | 1 |
| Wisconsin | 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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of May 28, 2021.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.