CLASS II Food recall · Reported 26 Sep 2012 · FDA Enforcement Report
Tomato/Basil Pressed Tortillas, 1 Dozen recalled
R & S Mexican Food Products is recalling Tomato/Basil Pressed Tortillas, 1 Dozen, distributed in Arizona. The recall was initiated on 3 Apr 2012 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-2348-2012
- FDA event ID
- 62873
- Recalling firm
- R & S Mexican Food Products, Glendale, AZ
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 3 Apr 2012
- FDA classified
- 19 Sep 2012
- Reported
- 26 Sep 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Allergens
- Product category
- Bread
Timeline
| 3 Apr 2012 | Recall initiated by company | |
| 19 Sep 2012 | Classified by FDA | +169 days |
| 26 Sep 2012 | 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
Product contains undeclared FD&C Yellow # 6.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
R&S Mexican Food Products, Inc. Tomato/Basil Pressed Tortillas, 1 Dozen. Packaged in sealed flexible plastic bag.
Where it was distributed
4 direct accounts in AZ. No international or outside states.
Questions about this recall
Why was it recalled?
Product contains undeclared FD&C Yellow # 6.
Which lots are affected?
No UPC or manufacturing code used.
Where was it sold?
4 direct accounts in AZ. No international or outside states.
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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