CLASS I Food recall · Reported 8 Apr 2015 · FDA Enforcement Report
BAM124 Chili Powder Salt Free recalled by Starwest Botanicals
Starwest Botanicals is recalling BAM124 Chili Powder Salt Free, distributed in Missouri. The recall was initiated on 14 Jan 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-1864-2015
- FDA event ID
- 70315
- Recalling firm
- Starwest Botanicals, Sacramento, CA
- Brand
- BAM124 Chili
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 14 Jan 2015
- FDA classified
- 1 Apr 2015
- Reported
- 8 Apr 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Spices
Timeline
| 14 Jan 2015 | Recall initiated by company | |
| 1 Apr 2015 | Classified by FDA | +77 days |
| 8 Apr 2015 | 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
Notified by immediate supplier of recall of ground cumin from Turkey due to the presence of peanut protein.
Product as listed by the FDA
BAM124 Chili Powder Salt Free
Where it was distributed
One customer in MO
Questions about this recall
Is BAM124 Chili Powder Salt Free recalled?
Yes. Starwest Botanicals recalled BAM124 Chili Powder Salt Free on 14 Jan 2015. The recall is Class I and its status is Terminated. Recall number F-1864-2015.
Why was it recalled?
Notified by immediate supplier of recall of ground cumin from Turkey due to the presence of peanut protein.
Which lots are affected?
Lot 11950-71
Where was it sold?
One customer in MO
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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