CLASS I Food recall · Reported 18 Dec 2019 · FDA Enforcement Report
Fresh From Meijer vegetable tray recalled
Meijer is recalling Fresh From Meijer vegetable tray, distributed in Illinois, Indiana, Kentucky, Michigan, Ohio, Wisconsin. The recall was initiated on 4 Nov 2019 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
Timeline
| 4 Nov 2019 | Recall initiated by company | |
| 11 Dec 2019 | Classified by FDA | +37 days |
| 18 Dec 2019 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Listeria Monocytogenes
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Fresh From Meijer vegetable tray with UPC 2-20185-00000-2 and PLU 1592, packed in clear plastic sectioned container
Where it was distributed
all Meijer stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin.
IllinoisIndianaKentuckyMichiganOhioWisconsin
Stores named: Meijer
Questions about this recall
Is Fresh From Meijer vegetable tray recalled?
Yes. Meijer recalled Fresh From Meijer vegetable tray on 4 Nov 2019. The recall is Class I and its status is Terminated. Recall number F-0323-2020.
Why was it recalled?
Listeria Monocytogenes
Which lots are affected?
Sell By Sept 25, 2019 through Nov 8, 2019
Where was it sold?
all Meijer stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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