CLASS I Food recall · Reported 18 Mar 2020 · FDA Enforcement Report
Sunny Select Au Jus Gravy Mix pouch (24 pouches) recalled
McCormick & Company, Inc. - Flavor Manufacturing Center is recalling Sunny Select Au Jus Gravy Mix pouch (24 pouches), distributed in California, Nevada. The recall was initiated on 28 Jan 2020 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-0799-2020
- FDA event ID
- 84939
- Recalling firm
- McCormick & Company, Inc. - Flavor Manufacturing Center, Hunt Valley, MD
- Brand
- Sunny
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 Jan 2020
- FDA classified
- 6 Mar 2020
- Reported
- 18 Mar 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Milk
- Product category
- Sauces & Condiments
Timeline
| 28 Jan 2020 | Recall initiated by company | |
| 6 Mar 2020 | Classified by FDA | +38 days |
| 18 Mar 2020 | 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
Product being recalled due to undeclared milk.
Product as listed by the FDA
Sunny Select Au Jus Gravy Mix 1 OZ pouch (24 pouches per case)
Where it was distributed
The brand owner, Save Mart Supermarkets, has stores in California and Nevada . Product went too Distribution Center in California .
Questions about this recall
Why was it recalled?
Product being recalled due to undeclared milk.
Which lots are affected?
UPC: 717544135500 Date Codes: BEST BY DEC 08 2021 H and BEST BY DEC 09 2021 H
Where was it sold?
The brand owner, Save Mart Supermarkets, has stores in California and Nevada . Product went too Distribution Center in California .
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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