FDA Recall United States Terminated Historical recordClass II
Sprout's Farmers Market
- Product
- Sprouts Farmers Market Organic Cut Leaf Spinach, Net Wt 16 O…
- Published
- July 24, 2019
- Distribution
- The product was shipped from the manufac…
Sprout's Farmers Market Recall: Testing revealed the presence of Listeria monocytogenes in the frozen spinach
United States
TerminatedClass II
- Company
- Sprout's Farmers Market
- Product
- Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb)…
- Recall date
- June 14, 2019
- Terminated
- September 3, 2019
- Source
- FDA
Reason for recall
Testing revealed the presence of Listeria monocytogenes in the frozen spinach
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb), 453 g, Manufactured exclusively for Sprouts Farmers Market, Phoenix, AZ UPC 8 74875 00982 2, packaged in plastic bags, 12 bags per case. | Not published in this source record | 1,046 cases | USE BY 12 03 21 19031203A03 USA |
Distribution
- The product was shipped from the manufacturer to a food distributor for distribution exclusively to Sprouts Farmers Market grocery stores in the following states: AZ
- CA
- NV
- UT
- NM
- CO
- TX
- KS
- OK
- MO
- TN
- AL
- GA
- FL
- SC
- NC
- PA
- MD
- and VA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1553-2019
- Event ID
- 83147
- Status
- Terminated
- Classification
- Class II
- Company
- Sprout's Farmers Market
- Product description
- Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb), 453 g, Manufactured exclusively for Sprouts Farmers Market, Phoenix, AZ UPC 8 74875 00982 2, packaged in plastic bags, 12 bags per case.
- Quantity
- 1,046 cases
- Reason
- Testing revealed the presence of Listeria monocytogenes in the frozen spinach
- Recall initiation date
- June 14, 2019
- Report date
- July 24, 2019
- Classification date
- Not published in this source record
- Termination date
- September 3, 2019
- Distribution pattern
- The product was shipped from the manufacturer to a food distributor for distribution exclusively to Sprouts Farmers Market grocery stores in the following states: AZ, CA, NV, UT, NM, CO, TX, KS, OK, MO, TN, AL, GA, FL, SC, NC, PA, MD, and VA.
- UPC, lot, and code information
- USE BY 12 03 21 19031203A03 USA
- 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
Other products recalled under this same event
This recall shares FDA event ID 83147 with 1 other product entry in Public Health Trace.
Responsible company: Sprout's Farmers Market
Other recalls from Sprout's Farmers Market
FDA Recall United States Terminated Historical recordClass III
Sprout's Farmers Market
- Product
- Sprouts Farmers Market Saltine Crackers Sea Salt Tops NET WT…
- Published
- March 29, 2023
- Distribution
- Distributors in AZ, CA, GA
FDA Recall United States Terminated Historical recordClass II
Sprout's Farmers Market
- Product
- Sprouts Farmers Market Organic Cut Leaf Spinach, Net Wt 16 O…
- Published
- July 24, 2019
- Distribution
- The product was shipped from the manufac…
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 |
|---|---|
| Arizona | 1 |
| California | 1 |
| Nevada | 1 |
| Utah | 1 |
| New Mexico | 1 |
| Colorado | 1 |
| Texas | 1 |
| Kansas | 1 |
| Oklahoma | 1 |
| Missouri | 1 |
| Tennessee | 1 |
| Alabama | 1 |
| Georgia | 1 |
| Florida | 1 |
| South Carolina | 1 |
| North Carolina | 1 |
| Pennsylvania | 1 |
| Maryland | 1 |
| Virginia | 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 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.
