Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods Inner-packag
Summary
The FDA issued a Class II for Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 05 by Gimme Coffee, Inc.. Reason: Undeclared caffeine.
Details
Source
Food Recall
External ID
H-0303-2026
Action Date
2025-12-17
Status
Ongoing
Category
food
Product Description
Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods Inner-packaging/pod packaging: gimme! coffee Deep Disco caffeinated coffee pods
Lot/Code Info: Best by 09-30-2025 printed on the Deep Disco pod packaging. Best by 10-15-2025 printed on the Decaf pods.
Quantity Affected: 252 boxes
Reason for Recall
Undeclared caffeine
Distribution
FL, IA, MA, MD, MO, NC, NJ, NY, OH, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-24
Company
Ithaca, NY
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 105 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 (Gimme Coffee, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gimme Coffee, Inc. have FDA actions?
This is the only FDA action we have on record for Gimme Coffee, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0303-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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