Gose con Sandia, Sour Ale with watermelon, limes and sea salt, 12 oz. Can 6 pk. (72 oz. total) Can UPC 7 96363 00495
Summary
The FDA issued a Class II for Gose con Sandia, Sour Ale with watermelon, limes and sea salt, 12 oz. Can 6 pk by Avery Brewing Company. Reason: Due to over pressurization, can may fail/explode..
Details
Source
Food Recall
External ID
F-1021-2023
Action Date
2023-07-12
Status
Terminated
Category
food
Product Description
Gose con Sandia, Sour Ale with watermelon, limes and sea salt, 12 oz. Can 6 pk. (72 oz. total) Can UPC 7 96363 00495 2, Carton UPC 7 96363 00495 2 (6 cans per carton, 4 cartons per case)
Lot/Code Info: Date Code: Canned on: 01/20/23 Batch Code: 3918
Quantity Affected: 1078.25 cases (6 cans/carton, 4 cartons/case)
Reason for Recall
Due to over pressurization, can may fail/explode.
Distribution
AZ, CO, IN, IL, KY, MO, ND, OK, PA, SC, TN, UT, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-03
Company
Boulder, CO
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 228 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 (Avery Brewing Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Avery Brewing Company have FDA actions?
This is the only FDA action we have on record for Avery Brewing Company in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1021-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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