Meijer Brand Mushrooms, imported from The Netherlands Stems & Pieces, DR WT 4-oz and…
Meijer Distribution, Inc recalled this product and the FDA reported the enforcement action on 19 September 2012 as Class III. The recall was initiated by the firm. The sodium in the product is above the declared value of the sodium stated on the label.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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
- UPC
- 713733375450
- Reason for recall
- The sodium in the product is above the declared value of the sodium stated on the label.
- Recalling firm
- Meijer Distribution, Inc
- Firm location
- Grand Rapids, Michigan, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-2296-2012
- Quantity
- 74,667 units of 4-oz and 159,349 units of 8-oz
- Distribution
- 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.
- Initiated
- 16 August 2012
- Reported by FDA
- 19 September 2012
- Terminated
- 26 August 2013
- Firm notified by
- Letter
- Product codes
- All lots
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 12 months, from 16 August 2012 to termination on 26 August 2013. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 5 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Other records from Meijer Distribution, Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 47 other records name this firm.
All 48 records for Meijer Distribution, Inc
All 2012 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.