CLASS II Food recall · Reported 6 Sep 2017 · FDA Enforcement Report
(a) Seven Sundays Vanilla Cherry Pecan Muesli recalled
Garden Of Light is recalling (a) Seven Sundays Vanilla Cherry Pecan Muesli, distributed nationwide in the US. The recall was initiated on 14 Aug 2017 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-3470-2017
- FDA event ID
- 77947
- Recalling firm
- Garden Of Light, East Hartford, CT
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 14 Aug 2017
- FDA classified
- 30 Aug 2017
- Reported
- 6 Sep 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Cereal
Timeline
| 14 Aug 2017 | Recall initiated by company | |
| 30 Aug 2017 | Classified by FDA | +16 days |
| 6 Sep 2017 | 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
Product labeled containing pecans actually contains almonds
Product as listed by the FDA
(a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 2oz. cup UPC: 8-56088-00311-8
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Product labeled containing pecans actually contains almonds
Which lots are affected?
a)LOT CODES: JUNE 29,2018 & AUGUST 11,2018 (b) LOT CODES: AUGUST 11, 2018
Where was it sold?
Nationwide
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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