CLASS I Food recall · Reported 14 Dec 2016 · FDA Enforcement Report
Almonds Salted Caramel recalled by Meijer
Meijer is recalling Almonds Salted Caramel, distributed in 7 states. The recall was initiated on 7 Nov 2016 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
- Recall number
- F-0669-2017
- FDA event ID
- 75635
- Recalling firm
- Meijer, Grand Rapids, MI
- Brand
- Almonds
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 7 Nov 2016
- FDA classified
- 8 Dec 2016
- Reported
- 14 Dec 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Peanuts
- Product category
- Candy
Timeline
| 7 Nov 2016 | Recall initiated by company | |
| 8 Dec 2016 | Classified by FDA | +31 days |
| 14 Dec 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Meijer initiated a voluntary recall of Meijer Almonds Salted Caramel on 11/7/2016 due to undeclared allergen peanuts.
Product as listed by the FDA
Meijer Almonds Salted Caramel, 14 oz. packaged in plastic pouches
Where it was distributed
Domestic:IN, IL, KY, MI, OH, WI Foreign: None VA/DOD: None
IllinoisIndianaKentuckyMichiganOhioVirginiaWisconsin
Stores named: Meijer
Questions about this recall
Why was it recalled?
Meijer initiated a voluntary recall of Meijer Almonds Salted Caramel on 11/7/2016 due to undeclared allergen peanuts.
Which lots are affected?
UPC: 7-19283-23759-0
Where was it sold?
Domestic:IN, IL, KY, MI, OH, WI Foreign: None VA/DOD: None
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 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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