“Starbucks Vanilla Frappuccino Chilled Coffee Drink Recall: Foreign Glass Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/11952-starbucks-vanilla-frappuccino-chilled-coffee-drink-recall-foreign-glass-hazard. Based on FDA recall #F-0352-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0352-2023%22&limit=1).
Pepsico Inc, on behalf of Starbucks Coffee Company, recalled Starbucks Frappuccino Vanilla Chilled Coffee Drink due to a foreign glass hazard. The Food and Drug Administration announced the voluntary Class II recall on Jan. 28, 2023.
The recalled product contains a foreign object, specifically glass. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Pepsico Inc has 13 other recalls on record since 2018-03-14. Other recent recalls of similar products include Lipton Green Tea Citrus Recall (2025-09-17), Pepsico Recalls Root Beer Cans Due to Sugar Labeling Error (2024-03-22), and Schweppes Zero Sugar Ginger Ale Caffeine Free Recall (2024-03-09). Other recent recalls of similar products include Lactalis Canada Vanilla Creme Brulee Recall (2026-04-14), JFE Dumpling Party Trays Recall (2026-03-05), and Chilli Spanish Peanuts Recall (2026-03-12).
How to tell if you have this one
Check for the UPC code 012000813313 on the product label. The product is a 13.7 fl oz (405mL) Vanilla Frappuccino Chilled Coffee Drink from Starbucks Coffee Company.
Brand
Starbucks
Product
Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 Fl Oz (405mL). UPC 0 12000-81331 3. Starbucks Coffee Company
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Product
Immediately stop using the Vanilla Frappuccino Chilled Coffee Drink if it has the UPC 012000813313.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “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 6 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-0352-2023 (January 28, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0352-2023 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.