CLASS I Food recall · Reported 15 Apr 2015 · FDA Enforcement Report
Ground Cumin-ETO treated recalled by Myc Ingredients
Myc Ingredients is recalling MYC Ingredients, Inc. Ground Cumin-ETO treated, distributed in New Jersey, New York. The recall was initiated on 24 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-1906-2015
- FDA event ID
- 70213
- Recalling firm
- Myc Ingredients, Forest Hills, NY
- Brand
- MYC Ingredients
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 24 Dec 2014
- FDA classified
- 6 Apr 2015
- Reported
- 15 Apr 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Peanuts
- Product category
- Spices
Timeline
| 24 Dec 2014 | Recall initiated by company | |
| 6 Apr 2015 | Classified by FDA | +103 days |
| 15 Apr 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
MYC Ingredients, Inc. Ground Cumin-ETO treated, NET WT 50 LBS. DISTRIBUTED BY: MYC Ingredients 718-793-3310
Where it was distributed
NJ, NY
Questions about this recall
Is Ground Cumin-ETO treated recalled?
Yes. Myc Ingredients recalled Ground Cumin-ETO treated on 24 Dec 2014. The recall is Class I and its status is Terminated. Recall number F-1906-2015.
Why was it recalled?
Cumin may contain undeclared peanut protein.
Which lots are affected?
Lot Numbers: M-5379C, 2927 E, 2808E, M-5360A, 2948E, 2686E
Where was it sold?
NJ, 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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