Lower riskFood recall · FDA · Published August 15, 2022
Starbucks Vanilla Espresso Triple Shot Recall: Possible Metal Fragments Contamination
PepsiCo recalls 12-bottle cases of Starbucks Vanilla Espresso Triple Shot (15 oz) due to possible metal fragments. Consumers should check if they own this product and follow official instructions.
“Starbucks Vanilla Espresso Triple Shot Recall: Possible Metal Fragments Contamination.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/12392-starbucks-vanilla-espresso-triple-shot-recall-possible-metal-fragments-contamination. Based on FDA recall #F-1724-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1724-2022%22&limit=1).
Pepsico Inc, on behalf of Starbucks, recalled Starbucks Vanilla Espresso Triple Shot (15 oz) due to possible metal fragment contamination, the FDA said on Aug. 15, 2022.
How to tell if you have it
Starbucks Vanilla Espresso Triple Shot, 15 oz
12 bottles per case
221 cases
The hazard
The product poses a hazard of possible contamination by foreign material, specifically metal fragments.
Context
GovInfoNow's records show Pepsico Inc has had 13 other recalls since March 14, 2018. Other recent recalls include Lipton Green Tea Citrus Recall (Sept. 17, 2025) and Pepsico Recalls Root Beer Cans Due to Sugar Labeling Error (March 22, 2024). Similar product recalls include Ukrop's Bread Pudding with Vanilla Sauce Recall (July 30, 2026) and Straus Family Creamery Cookie Dough Ice Cream Recall (May 12, 2026).
How to tell if you have this one
Check for 12-bottle cases of Starbucks Vanilla Espresso Triple Shot (15 oz) with the product name and size listed on the bottle.
Brand
Starbucks
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product
Look for 12-bottle cases of Starbucks Vanilla Espresso Triple Shot (15 oz) with the product name and size listed on the bottle.
Where it went and when
Where it was distributed
Distributed in 7 states.
Listed by the agency
Not listed
FDA distribution: “Distributed to retail stores in AR, AZ, FL, IL, IN, OK, TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
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-1724-2022 (August 15, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1724-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.