Class IIOngoingVoluntary: Firm initiated
Gimme Coffee, Inc.: food recall H-0303-2026
Gimme Coffee, Inc. of Ithaca, NY recalled Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods… Reason: Undeclared caffeine. The FDA listed it as Class II in its Enforcement Report dated Dec 17, 2025; distribution: Florida, Iowa, Massachusetts, Maryland, Missouri, North Carolina, New Jersey, New York, Ohio, Wisconsin.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 252 boxes
- Reason for recall
- Undeclared caffeine
- Codes, lots and dates on the package
- Best by 09-30-2025 printed on the Deep Disco pod packaging. Best by 10-15-2025 printed on the Decaf pods.
- Distribution pattern
- FL, IA, MA, MD, MO, NC, NJ, NY, OH, WI
- Recalling firm
- Gimme Coffee, Inc., Ithaca, NY
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 24, 2025 |
| Classified by the FDA | Dec 11, 2025 |
| Published in the Enforcement Report | Dec 17, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0303-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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