Recall events
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Event 88775
Event summary
Timeline bucket September 26, 2021
Product types Food
Classifications Class II
Statuses Terminated
Recalling firm wording Pepsico Inc
Dossier provenance
Source snapshots represented here
openFDA Food Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
3 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
food · product 1 of 3
Starbucks Doubleshot Espresso, Espresso & Cream, 6.5 FL OZ UPC 012000001772
F-0089-2022
Recall number F-0089-2022
Initiated September 26, 2021
Classification Class II
Status Terminated
Quantity 85,956 cases (total)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
Code information MAR 28 22
Distribution pattern Distributed to retailers nationwide.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[24953]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 3
Starbucks Doubleshot Espresso, Espresso & Light Cream, 6.5 FL OZ UPC 012000008801
F-0090-2022
Recall number F-0090-2022
Initiated September 26, 2021
Classification Class II
Status Terminated
Quantity 85,956 cases (total)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
Code information MAR 28 22
Distribution pattern Distributed to retailers nationwide.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[23565]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 3
Starbucks Doubleshot Espresso, Espresso & Salted Caramel Cream, 6.5 FL OZ UPC 012000007293
F-0091-2022
Recall number F-0091-2022
Initiated September 26, 2021
Classification Class II
Status Terminated
Quantity 85,956 cases (total)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
Code information MAR 28 22
Distribution pattern Distributed to retailers nationwide.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[24957]
FDA event record
· Exact recall-number query on openFDA