Patagonia Foods 3610100 Blackberry IQF Product of Mexico Net Wt. 30 LBS. (13.61 kg) Production/Lot Code 20422 Distribute
Summary
The FDA issued a Class I for Patagonia Foods 3610100 Blackberry IQF Product of Mexico Net Wt. 30 LBS. (13.61 by PATAGONIA FOOD LLC. Reason: Possible Hepatitis A in blackberries.
Details
Source
Food Recall
External ID
F-0760-2023
Action Date
2023-05-03
Status
Terminated
Category
food
Product Description
Patagonia Foods 3610100 Blackberry IQF Product of Mexico Net Wt. 30 LBS. (13.61 kg) Production/Lot Code 20422 Distributed By: Patagonia Foods, LLC. San Luis Obispo, CA 93401 patagoniafoods.com
Lot/Code Info: Lot Code: 20422
Quantity Affected: N/A
Reason for Recall
Possible Hepatitis A in blackberries
Distribution
U.S. distribution to the following: CA, OR, NE, TX, WA, NV No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-17
Company
San Luis Obispo, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
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 I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (PATAGONIA FOOD LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does PATAGONIA FOOD LLC have FDA actions?
This is the only FDA action we have on record for PATAGONIA FOOD LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0760-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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