Starbucks recalls Doubleshot Espresso and Light Cream products due to potential premature spoilage from sealing issues. Consumers should check UPC 012000008801 for affected items.
“Starbucks Doubleshot Espresso Recall: Premature Spoilage Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/14097-starbucks-doubleshot-espresso-recall-premature-spoilage-risk. Based on FDA recall #F-0090-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0090-2022%22&limit=1).
Pepsico Inc recalled Starbucks Doubleshot Espresso and Espresso & Light Cream, 6.5 FL OZ due to inadequate sealing that may cause premature spoilage, the FDA said on Sept. 26, 2021.
An issue with adequate sealing of canned coffee products potentially leads to premature spoilage.
Context
Pepsico Inc has 14 other recalls on record since March 14, 2018. Other recent recalls of similar products include Gatorade Recall: Undeclared Yellow No. 5/6 in 28 oz Bottles (Sept. 25, 2026), Lipton Green Tea Citrus Recall: Undeclared Sugar in Bottles (Sept. 17, 2025), and Pepsico Recalls Root Beer Cans Due to Sugar Labeling Error (March 22, 2024).
How to tell if you have this one
Check for the UPC code 012000008801 on the product label. The recall applies to Starbucks Doubleshot Espresso and Light Cream products sold around March 28, 2022.
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
Distributed to retailers nationwide.
Recall number
Product, codes & lots
F-0089-2022
Starbucks Doubleshot Espresso, Espresso & Cream, 6.5 FL OZ UPC 012000001772; MAR 28 22
F-0090-2022
Starbucks Doubleshot Espresso, Espresso & Light Cream, 6.5 FL OZ UPC 012000008801; MAR 28 22
F-0091-2022
Starbucks Doubleshot Espresso, Espresso & Salted Caramel Cream, 6.5 FL OZ UPC 012000007293; MAR 28 22
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC code 012000008801 on the product label to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Distributed to retailers nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
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 #F-0090-2022 (September 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0090-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.