CLASS II Food recall · Reported 11 Sep 2013 · FDA Enforcement Report
H-e-b Jumbo Butterfly Shrimp recalled by The Seafood Exchange Of Fla
The Seafood Exchange Of Fla is recalling H-e-b Jumbo Butterfly Shrimp, distributed in Texas. The recall was initiated on 29 Aug 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-1870-2013
- FDA event ID
- 66146
- Recalling firm
- The Seafood Exchange Of Fla, Raleigh, NC
- Brand
- H-e-b
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 29 Aug 2013
- FDA classified
- 5 Sep 2013
- Reported
- 11 Sep 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Tree Nuts
- Product category
- Shrimp
Timeline
| 29 Aug 2013 | Recall initiated by company | |
| 5 Sep 2013 | Classified by FDA | +7 days |
| 11 Sep 2013 | 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
Cartons of this product have been found to contain coconut shrimp. Coconut is not listed as an ingredient.
Product as listed by the FDA
H-E-B Jumbo Butterfly Shrimp-10.5 oz Box, 20 units per case
Where it was distributed
TX
Stores named: H-E-B
Questions about this recall
Is H-e-b Jumbo Butterfly Shrimp recalled?
Yes. The Seafood Exchange Of Fla recalled H-e-b Jumbo Butterfly Shrimp on 29 Aug 2013. The recall is Class II and its status is Terminated. Recall number F-1870-2013.
Why was it recalled?
Cartons of this product have been found to contain coconut shrimp. Coconut is not listed as an ingredient.
Which lots are affected?
Product marked with "BEST BY 23APR2014"
Where was it sold?
TX
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 21 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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