Gimme Coffee recalls decaf coffee pods labeled as caffeine-free but contain undeclared caffeine. Affected pods have specific UPC and best-by dates. Consumers should check packaging for caffeine content.
“Gimme Coffee Decaf Pods Recall: Undeclared Caffeine Hazard.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6933-gimme-coffee-decaf-pods-recall-undeclared-caffeine-hazard. Based on FDA recall #H-0303-2026.
The FDA announced on November 24, 2025, that Gimme Coffee, Inc. voluntarily recalled gimme! brand Decaf de Agua coffee pods due to undeclared caffeine. The recall affects approximately 252 boxes distributed in Florida, Iowa, Massachusetts, Maryland, Missouri, North Carolina, New Jersey, New York, Ohio, and Wisconsin.
How to tell if you have it
gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods
The hazard
The outer-packaging labeled as 'Decaf de Agua' coffee pods actually contained caffeinated Deep Disco coffee pods. The undeclared caffeine poses a risk to consumers who may be sensitive to caffeine or have dietary restrictions requiring decaffeinated products.
Context
GovInfoNow's records show other recent recalls of similar products include McCafe Premium Roast Decaf K-Cup Pods May Contain Caffeine (2025-12-06) and Lost and Found Energy Sour Gummy Bear Recall: Incorrect Caffeine Label (2025-12-02). Loard's Coffee Ice also faced a recall for undeclared milk hazard in 32oz cans on 2026-04-15.
How to tell if you have this one
Check for the UPC 051497457990 on the outer packaging. The Decaf pods have a best-by date of 10-15-2025, while the caffeinated Deep Disco pods have a best-by date of 09-30-2025.
Brand
Gimme Coffee
Product
Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Packaging
Look for the UPC 051497457990 on the outer packaging of the coffee pods.
Where it went and when
Where it was distributed
Distributed in 10 states.
Listed by the agency
Not listed
FDA distribution: “FL, IA, MA, MD, MO, NC, NJ, NY, OH, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Iowa, Maryland, Massachusetts, Missouri, New Jersey, New York, North Carolina, Ohio, Wisconsin.
Recall timeline
FDA published this recall 23 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0303-2026 (November 24, 2025)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.