CLASS I Food recall · Reported 20 May 2015 · FDA Enforcement Report
Forest Bounty Grail Mix: Aurora recalled
Aurora Products is recalling Forest Bounty Grail Mix: Aurora, distributed nationwide in the US. The recall was initiated on 20 Mar 2015 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-2263-2015
- FDA event ID
- 70789
- Recalling firm
- Aurora Products, Orange, CT
- Brand
- Forest Bounty
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 20 Mar 2015
- FDA classified
- 12 May 2015
- Reported
- 20 May 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Salmonella
- Product category
- Other
Timeline
| 20 Mar 2015 | Recall initiated by company | |
| 12 May 2015 | Classified by FDA | +53 days |
| 20 May 2015 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Salmonella
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Forest Bounty Grail Mix: Aurora, 13 oz. Plastic Cup, UPC: 65585200571; Aurora, 13 oz. Plastic Pouch, UPC: 65585200290; Aurora, 17.5 oz. Plastic Cup, UPC: 65585200496
Where it was distributed
Product shipped to distributors in the following states: NY, CT, NH, RI, MA, CA, MD, ME, MN, PA and Nationwide through retail stores. Canada: Winners, HomeSense and Marshalls stores Bermuda
Nationwide CaliforniaConnecticutMassachusettsMarylandMaineMinnesotaNew HampshireNew YorkPennsylvaniaRhode Island
Questions about this recall
Is Forest Bounty Grail Mix: Aurora recalled?
Yes. Aurora Products recalled Forest Bounty Grail Mix: Aurora on 20 Mar 2015. The recall is Class I and its status is Terminated. Recall number F-2263-2015.
Why was it recalled?
Salmonella
Which lots are affected?
Best if used by date range: 10/28/15 12/13/15
Where was it sold?
Product shipped to distributors in the following states: NY, CT, NH, RI, MA, CA, MD, ME, MN, PA and Nationwide through retail stores. Canada: Winners, HomeSense and Marshalls stores Bermuda
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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|---|---|---|---|---|---|
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