CLASS I Food recall · Reported 18 Feb 2015 · FDA Enforcement Report
Cumin Seed, Ground, packed as recalled by Regional Access
Regional Access is recalling Cumin Seed, Ground, packed as, distributed in New York. The recall was initiated on 26 Dec 2014 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-1038-2015
- FDA event ID
- 70198
- Recalling firm
- Regional Access, Ithaca, NY
- Brand
- Cumin
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 26 Dec 2014
- FDA classified
- 9 Feb 2015
- Reported
- 18 Feb 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Peanuts
- Product category
- Spices
Timeline
| 26 Dec 2014 | Recall initiated by company | |
| 9 Feb 2015 | Classified by FDA | +45 days |
| 18 Feb 2015 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Cumin may contain undeclared peanut protein.
Product as listed by the FDA
Cumin Seed, Ground, packed as NET WT 1 lb, Reorder: #HS300, and NET WT 5 lb, Reorder: #HS310. Regional Access Inc. 607-319-5150, Email: [email protected]
Where it was distributed
NY
Questions about this recall
Is Cumin Seed, Ground, packed as recalled?
Yes. Regional Access recalled Cumin Seed, Ground, packed as on 26 Dec 2014. The recall is Class I and its status is Terminated. Recall number F-1038-2015.
Why was it recalled?
Cumin may contain undeclared peanut protein.
Which lots are affected?
Packed on: 7/29/2014
Where was it sold?
NY
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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