CLASS II Food recall · Reported 20 Jul 2022 · FDA Enforcement Report
Slap Ya Mama Louisiana Food Products Slap Ya Mama Cajun Fish Fry recalled
Walker & Sons is recalling Slap Ya Mama Louisiana Food Products Slap Ya Mama Cajun Fish Fry, distributed in Georgia, Tennessee, Texas. The recall was initiated on 23 Jun 2022 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-1412-2022
- FDA event ID
- 90515
- Recalling firm
- Walker & Sons, Ville Platte, LA
- Brand
- Slap Ya
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 23 Jun 2022
- FDA classified
- 11 Jul 2022
- Reported
- 20 Jul 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Fish
Timeline
| 23 Jun 2022 | Recall initiated by company | |
| 11 Jul 2022 | Classified by FDA | +18 days |
| 20 Jul 2022 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Wheat Allergen
Product as listed by the FDA
Slap Ya Mama Louisiana Food Products Slap Ya Mama Cajun Fish Fry packaged in a 5.5lb plastic container with plastic screw top - 4 units per case UPC 8 17885 00027 4
Where it was distributed
Georgia, Tennessee, Texas
Questions about this recall
Why was it recalled?
Undeclared Wheat Allergen
Which lots are affected?
Lot Numbers: 0504142201, 0505192201, 0505312202 Product Numbers: 817885000274
Where was it sold?
Georgia, Tennessee, Texas
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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