CLASS I Food recall · Reported 18 Feb 2015 · FDA Enforcement Report
Amana Dinner Rolls recalled by The Jefferson Street Bakery
The Jefferson Street Bakery is recalling Amana Dinner Rolls, distributed in Iowa, Illinois, Minnesota, Nebraska, South Dakota. The recall was initiated on 28 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-1197-2015
- FDA event ID
- 70403
- Recalling firm
- The Jefferson Street Bakery, Burlington, IA
- Brand
- Amana Dinner
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 Jan 2015
- FDA classified
- 11 Feb 2015
- Reported
- 18 Feb 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Milk
- Product category
- Bread
Timeline
| 28 Jan 2015 | Recall initiated by company | |
| 11 Feb 2015 | Classified by FDA | +14 days |
| 18 Feb 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
The products are being recalled due to the presence of undeclared milk allergens.
Product as listed by the FDA
Amana Dinner Rolls, packaged in 1 lb 2 oz plastic bags
Where it was distributed
Product distributed in Iowa, Illinois, Minnesota, Nebraska, and South Dakota.
Questions about this recall
Is Amana Dinner Rolls recalled?
Yes. The Jefferson Street Bakery recalled Amana Dinner Rolls on 28 Jan 2015. The recall is Class I and its status is Terminated. Recall number F-1197-2015.
Why was it recalled?
The products are being recalled due to the presence of undeclared milk allergens.
Which lots are affected?
834J364
Where was it sold?
Product distributed in Iowa, Illinois, Minnesota, Nebraska, and South Dakota.
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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