CLASS II Food recall · Reported 22 Feb 2023 · FDA Enforcement Report

Starbucks frappuccino Vanilla recalled by Pepsico

Pepsico is recalling Starbucks frappuccino Vanilla, distributed nationwide in the US. The recall was initiated on 28 Jan 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiration Dates: MAR 08 23, MAY 29 23, JUN 04 23, JUN 10, 23

Quantity recalled25,200 cases (12 bottles per case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0352-2023
FDA event ID: 91604
Recalling firm: Pepsico, Purchase, NY
Brand: Starbucks
Classification: Class II
Status: Terminated
Recall initiated: 28 Jan 2023
FDA classified: 14 Feb 2023
Reported: 22 Feb 2023
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Foreign Material
Product category: Coffee

Timeline

28 Jan 2023	Recall initiated by company
14 Feb 2023	Classified by FDA	+17 days
22 Feb 2023	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Foreign object (glass).

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 Fl Oz (405mL). UPC 0 12000-81331 3. Starbucks Coffee Company. For comments or questions, call 1-800-211-8307.

Where it was distributed

nationwide

Nationwide

Stores named: Starbucks

Questions about this recall

Why was it recalled?

Foreign object (glass).

Which lots are affected?

Expiration Dates: MAR 08 23, MAY 29 23, JUN 04 23, JUN 10, 23

Where was it sold?

nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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