Texas Olive Company Capers Capote 8 oz. plastic containers. All lots with expiry prior to 06/04/2025 Texas Olive Compa
Summary
The FDA issued a Class II for Texas Olive Company Capers Capote 8 oz. plastic containers. All lots with expir by All American Trading Of Houston, Inc.. Reason: The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed..
Details
Source
Food Recall
External ID
F-0727-2025
Action Date
2025-04-30
Status
Ongoing
Category
food
Product Description
Texas Olive Company Capers Capote 8 oz. plastic containers. All lots with expiry prior to 06/04/2025 Texas Olive Company Capers Capote 16 oz. glass jar. All lots with expiry prior to 12/21/2025
Lot/Code Info: All lots with expiry prior to 06/04/2025 (8 oz) All lots with expiry prior to 12/21/2025 (16 oz)
Quantity Affected: 3,124 units
Reason for Recall
The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
Distribution
Texas and Mississippi
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-04
Company
Houston, TX
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 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.
All American Trading Of Houston, Inc. has 3 FDA actions in our database, including 3 recalls.
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 (All American Trading Of Houston, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does All American Trading Of Houston, Inc. have FDA actions?
All American Trading Of Houston, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0727-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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