FDA Recall United States Terminated Historical recordClass I
Meijer Distribution, Inc
- Product
- Meijer Sharable Waldorf Salad 16 Oz retail unit in plastic…
- Published
- January 10, 2018
- Distribution
- Multiple states
Meijer Distribution, Inc Recall: Sliced apples within the products being potentially contaminated with Listeria monocytogenes.
United States
TerminatedClass I
- Company
- Meijer Distribution, Inc
- Product
- Meijer Fresh Cranberry Apple Stuffing Starter 18.9 Oz retai…
- Recall date
- December 18, 2017
- Terminated
- February 15, 2018
- Source
- FDA
Reason for recall
Sliced apples within the products being potentially contaminated with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Meijer Fresh Cranberry Apple Stuffing Starter 18.9 Oz retail unit in plastic container UPC: 7-19283-37977-1 4 retail containers per wholesale case | 7-19283-37977-1 | 768 retail units | printed labels include sell by range of December 17, 2017 through December 21, 2017 |
Distribution
- IL
- IN
- KY
- MI
- OH
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0615-2018
- Event ID
- 78805
- Status
- Terminated
- Classification
- Class I
- Company
- Meijer Distribution, Inc
- Product description
- Meijer Fresh Cranberry Apple Stuffing Starter 18.9 Oz retail unit in plastic container UPC: 7-19283-37977-1 4 retail containers per wholesale case
- Quantity
- 768 retail units
- Reason
- Sliced apples within the products being potentially contaminated with Listeria monocytogenes.
- Recall initiation date
- December 18, 2017
- Report date
- January 10, 2018
- Classification date
- Not published in this source record
- Termination date
- February 15, 2018
- Distribution pattern
- IL, IN, KY, MI, OH, WI
- UPC, lot, and code information
- UPC 7-19283-37977-1; printed labels include sell by range of December 17, 2017 through December 21, 2017
- 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 78805 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
Meijer Distribution, Inc
- Product
- Meijer Michigan Harvest Salad 10 Oz retail unit in plastic…
- Published
- January 10, 2018
- Distribution
- Multiple states
Responsible company: Meijer Distribution, Inc
Other recalls from Meijer Distribution, Inc
FDA Recall United States Terminated Historical recordClass II
Meijer Distribution, Inc
- Product
- Meijer Greek Yogurt 0% Blueberry 5.3 oz. The products are…
- Published
- March 7, 2018
- Distribution
- Domestic: Meijer stores in Michigan, Ohi…
FDA Recall United States Terminated Historical recordClass II
Meijer Distribution, Inc
- Product
- Meijer Greek Yogurt 0% Strawberry 5.3 oz. The products are…
- Published
- March 7, 2018
- Distribution
- Domestic: Meijer stores in Michigan, Ohi…
FDA Recall United States Terminated Historical recordClass II
Meijer Distribution, Inc
- Product
- Meijer Greek Yogurt 0% Vanilla 5.3 oz. The products are pac…
- Published
- March 7, 2018
- Distribution
- Domestic: Meijer stores in Michigan, Ohi…
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 |
|---|---|
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Michigan | 1 |
| Ohio | 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.
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.
