CLASS I Food recall · Reported 21 Jun 2017 · FDA Enforcement Report
Western Family Onion Soup Mix recalled by Gilster-Mary Lee
Gilster-Mary Lee is recalling Western Family Onion Soup Mix, distributed in Utah. The recall was initiated on 5 Jun 2017 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-2366-2017
- FDA event ID
- 77438
- Recalling firm
- Gilster-Mary Lee, Chester, IL
- Brand
- Western
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 5 Jun 2017
- FDA classified
- 9 Jun 2017
- Reported
- 21 Jun 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Egg
- Product category
- Soup
Timeline
| 5 Jun 2017 | Recall initiated by company | |
| 9 Jun 2017 | Classified by FDA | +4 days |
| 21 Jun 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The product may contain undeclared egg.
Product as listed by the FDA
Western Family Onion Soup Mix, 2.25 oz. pouches packaged in 4.5-oz. cartons
Where it was distributed
Domestic only: ASSOCIATED FOODS STORES FARR WEST WAREHOUSE 1850 WEST 2530 NORTH FARR WEST, UT 84404
Questions about this recall
Why was it recalled?
The product may contain undeclared egg.
Which lots are affected?
Western Family Onion Soup Mix, UPC 15400-03604, 2.25 oz. pouches packaged in 4.5-oz. cartons which have a Best By date of APR 10 18 D16
Where was it sold?
Domestic only: ASSOCIATED FOODS STORES FARR WEST WAREHOUSE 1850 WEST 2530 NORTH FARR WEST, UT 84404
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 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.
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