CLASS II Food recall · Reported 16 Apr 2014 · FDA Enforcement Report
Prego Italian Sauce Traditional recalled by Campbell Soup Supply Co
Campbell Soup Supply is recalling Prego Italian Sauce Traditional, distributed in Arkansas, Arizona, Kansas, Missouri, New Mexico, Oklahoma. The recall was initiated on 31 Dec 2013 and the FDA has classified it as Class II.
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-1748-2014
- FDA event ID
- 67195
- Recalling firm
- Campbell Soup Supply, Camden, NJ
- Brand
- Prego
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 31 Dec 2013
- FDA classified
- 4 Apr 2014
- Reported
- 16 Apr 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Mold
- Product category
- Sauces & Condiments
Timeline
| 31 Dec 2013 | Recall initiated by company | |
| 4 Apr 2014 | Classified by FDA | +94 days |
| 16 Apr 2014 | 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 may have become spoiled due to an elevated pH caused by dilute cleaning solution in the product.
Product as listed by the FDA
Prego Italian Sauce Traditional, NET WT. 24 OZ (1 LB. 80 Z.)(680 g) in glass jars.
Where it was distributed
AZ, NM, OK, AR, MO, NB, and KS
Questions about this recall
Why was it recalled?
Product may have become spoiled due to an elevated pH caused by dilute cleaning solution in the product.
Which lots are affected?
UPC 51000 2549 4, Expiration date JUN 16, 2015, Lid Codes JUN 16 2015 12153 CT BJ ZV 0330 through JUN 16 2015 12153 CT BJ ZV 0449
Where was it sold?
AZ, NM, OK, AR, MO, NB, and KS
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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