CLASS II Food recall · Reported 3 Apr 2013 · FDA Enforcement Report
Meijer, Spiced Jelly Beans recalled by Meijer Distribution
Meijer Distribution is recalling Meijer, Spiced Jelly Beans, distributed in Illinois, Indiana, Kentucky, Michigan, Ohio. The recall was initiated on 20 Mar 2013 and the FDA has classified it as Class II.
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
- Recall number
- F-1273-2013
- FDA event ID
- 64709
- Recalling firm
- Meijer Distribution, Grand Rapids, MI
- Brand
- Meijer
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 20 Mar 2013
- FDA classified
- 27 Mar 2013
- Reported
- 3 Apr 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Candy
Timeline
| 20 Mar 2013 | Recall initiated by company | |
| 27 Mar 2013 | Classified by FDA | +7 days |
| 3 Apr 2013 | 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
32 oz bags of Meijer Spiced Jelly Beans contain undeclared Yellow # 6.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Meijer, Spiced Jelly Beans, 32 oz, Product of Mexico, UPC 8-86926-50931-1.
Where it was distributed
Meijer stores in IL, IN, MI, OH, KY
IllinoisIndianaKentuckyMichiganOhio
Stores named: Meijer
Questions about this recall
Why was it recalled?
32 oz bags of Meijer Spiced Jelly Beans contain undeclared Yellow # 6.
Which lots are affected?
all lots
Where was it sold?
Meijer stores in IL, IN, MI, OH, KY
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 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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