CLASS II Food recall · Reported 3 Jun 2015 · FDA Enforcement Report
Turtle Island Roast Beef Spice Blend, stock recalled
Regency Group, Inc., The is recalling Turtle Island Roast Beef Spice Blend, stock, distributed in 8 states. The recall was initiated on 30 Apr 2015 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-2339-2015
- FDA event ID
- 71141
- Recalling firm
- Regency Group, Inc., The, Portland, OR
- Brand
- Turtle Island
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Apr 2015
- FDA classified
- 28 May 2015
- Reported
- 3 Jun 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Beef
Timeline
| 30 Apr 2015 | Recall initiated by company | |
| 28 May 2015 | Classified by FDA | +28 days |
| 3 Jun 2015 | 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
Turtle Island Roast Beef Spice Blend is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
Product as listed by the FDA
Turtle Island Roast Beef Spice Blend, stock code 12690, packaged in 25 lbs.container. No UPC
Where it was distributed
distributed in AK, AZ, CA, ID, MT, OR, UT and WA.
Questions about this recall
Why was it recalled?
Turtle Island Roast Beef Spice Blend is recalled due to contamination with gluten (wheat allergen) and label does not declare wheat.
Which lots are affected?
Lot 12690-150227
Where was it sold?
distributed in AK, AZ, CA, ID, MT, OR, UT and WA.
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.
Other products in this recall event
10 other products · FDA event 71141This product is part of a recall event; the main page for the event is Oregano, Mediterranean ground, stock recalled.
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|---|---|---|---|---|---|
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