CLASS II Food recall · Reported 22 Oct 2025 · FDA Enforcement Report
Good and Gather Southwest-Style Burrito Bowl Blend recalled
One Frozen is recalling Good and Gather Southwest-Style Burrito Bowl Blend Processed in a facility that also, distributed nationwide in the US. The recall was initiated on 4 Sep 2025 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
- H-0042-2026
- FDA event ID
- 97572
- Recalling firm
- One Frozen, Rochester, NY
- Brand
- Gather
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 4 Sep 2025
- FDA classified
- 10 Oct 2025
- Reported
- 22 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Fish & Shellfish
- Product category
- Ready Meals
Timeline
| 4 Sep 2025 | Recall initiated by company | |
| 10 Oct 2025 | Classified by FDA | +36 days |
| 22 Oct 2025 | 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 contain undeclared shrimp (crustacean shellfish).
Product as listed by the FDA
Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in a facility that also handles shellfish, egg, fish, milk, sesame, soy, tree nut and wheat ingredients
Where it was distributed
Nationwide.
Stores named: Target
Questions about this recall
Why was it recalled?
Product may contain undeclared shrimp (crustacean shellfish).
Which lots are affected?
Lot: 5505-1 and 5505-2
Where was it sold?
Nationwide.
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.