Southern Belle Seafood Crabmeat Stuffing, Packed: 2/25 lb. Bag, Net Weight: 50 lb. (22.68 kg), Use By: 08/23/2023
Summary
The FDA issued a Class II for Southern Belle Seafood Crabmeat Stuffing, Packed: 2/25 lb. Bag, Net Weight: 50 l by Shaw's Southern Belle Frozen Foods, Inc.. Reason: A piece of brittle plastic was found in seafood crabmeat stuffing mix..
Details
Source
Food Recall
External ID
F-1507-2023
Action Date
2023-09-20
Status
Terminated
Category
food
Product Description
Southern Belle Seafood Crabmeat Stuffing, Packed: 2/25 lb. Bag, Net Weight: 50 lb. (22.68 kg), Use By: 08/23/2023
Lot/Code Info: Use By: 08/23/2023 Lot # 042504
Quantity Affected: 600 lbs
Reason for Recall
A piece of brittle plastic was found in seafood crabmeat stuffing mix.
Distribution
Domestic distribution only.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-14
Company
Jacksonville, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Shaw's Southern Belle Frozen Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Shaw's Southern Belle Frozen Foods, Inc. have FDA actions?
This is the only FDA action we have on record for Shaw's Southern Belle Frozen Foods, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1507-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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