CLASS II Food recall · Reported 6 Oct 2021 · FDA Enforcement Report
Grab & Go Bistro Pimento Cheese Sandwich 1 sandwich per package recalled
Modern Distributors is recalling Grab & Go Bistro Pimento Cheese Sandwich 1 sandwich per package, distributed in Kentucky. The recall was initiated on 27 Jul 2021 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-1026-2021
- FDA event ID
- 88633
- Recalling firm
- Modern Distributors, Somerset, KY
- Brand
- Grab
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 27 Jul 2021
- FDA classified
- 30 Sep 2021
- Reported
- 6 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Visit
- Reason category
- Undeclared Fish & Shellfish
- Product category
- Ready Meals
Timeline
| 27 Jul 2021 | Recall initiated by company | |
| 30 Sep 2021 | Classified by FDA | +65 days |
| 6 Oct 2021 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Fish not declared as an allergen
Product as listed by the FDA
Grab & Go Bistro Pimento Cheese Sandwich 5oz plastic container 1 sandwich per package
Where it was distributed
Distributed to firm owned vending machines within Kentucky
Questions about this recall
Why was it recalled?
Fish not declared as an allergen
Which lots are affected?
UPC 000000999281 ID 99928
Where was it sold?
Distributed to firm owned vending machines within Kentucky
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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