Food recall
Meijer Distribution, Inc recall: Meijer Brand Mushrooms, imported from The Netherlands Stems & Pieces, DR WT 4-oz and 8-oz sizes/Net Wt
Meijer Distribution, Inc, of Grand Rapids, MI, recalled Meijer Brand Mushrooms, imported from The Netherlands Stems & Pieces, DR WT 4-oz and 8-oz sizes/Net Wt. The FDA's reason: “The sodium in the product is above the declared value of the sodium stated on the label.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on August 16, 2012, and the FDA first listed it in its Enforcement Report of September 19, 2012. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class III
It is unlikely to cause harm
Why
Labeling, packaging or manufacturing problems
Status
Terminated
Closed August 26, 2013
The recall
- Company
- Meijer Distribution, Inc (Grand Rapids, MI)
- Reason, in FDA's words
- “The sodium in the product is above the declared value of the sodium stated on the label.”
- Where it was sold
- The 4 oz. product was distributed to 25 stores and the. 8 oz. product was distributed to 197 stores. Stores are located in Illinois, Indiana, Kentucky, Michigan, and Ohio. Product was distributed from Meijer's distribution centers located in lansing, Michigan; Newport, Michigan; and Tipp City, Ohio.
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 62890
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-2296-2012 Class III
Meijer Brand Mushrooms, imported from The Netherlands Stems & Pieces, DR WT 4-oz and 8-oz sizes/Net Wt. 6.5-oz and 13.25-oz, UPC 7-1373337545-0 and UPC 7-1373337544-3
Codes: All lots
Quantity: 74,667 units of 4-oz and 159,349 units of 8-oz
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of September 19, 2012.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.