Recall events
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Event 81492
Event summary
Timeline bucket October 30, 2018
Product types Food
Classifications Class II
Statuses Terminated
Recalling firm wording Luckyberry
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
9 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 9
Luckyberry Cold-Pressed Juice, NoCoast, Kale, Cucumber, Green Apple, Celery, Lemon, Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0766-2019
Recall number F-0766-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 3 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[3964]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 9
Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0767-2019
Recall number F-0767-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 4 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[4192]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 9
Luckyberry Cold-Pressed Juice, Clean & Clear, Pineapple, Green Apple, Cucumber, Min, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0768-2019
Recall number F-0768-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 7 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[2901]
FDA event record
· Exact recall-number query on openFDA
food · product 4 of 9
Luckyberry Cold-Pressed Juice, Merc Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0769-2019
Recall number F-0769-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 9 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[3957]
FDA event record
· Exact recall-number query on openFDA
food · product 5 of 9
Luckyberry Cold-Pressed Juice, Spicy Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0770-2019
Recall number F-0770-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 6 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[2911]
FDA event record
· Exact recall-number query on openFDA
food · product 6 of 9
Luckyberry Cold-Pressed Juice, Seasonal Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0771-2019
Recall number F-0771-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 5 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[3948]
FDA event record
· Exact recall-number query on openFDA
food · product 7 of 9
Luckyberry Cold-Pressed Juice, Beetnik, Orange, Red Beet, Kale, Cucumber, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0772-2019
Recall number F-0772-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 3 bottles.
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[2842]
FDA event record
· Exact recall-number query on openFDA
food · product 8 of 9
Luckyberry Cold-Pressed Juice, Spicy Watermelon, Watermelon, Red Beet, Lime, Mint, Green Apple, Jalepeno, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0773-2019
Recall number F-0773-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 5 bottles.
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[4183]
FDA event record
· Exact recall-number query on openFDA
food · product 9 of 9
Luckyberry Cold-Pressed Juice, Mai Tai, Orange Pineapple, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
F-0774-2019
Recall number F-0774-2019
Initiated October 30, 2018
Classification Class II
Status Terminated
Quantity At least 1 bottle.
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Distribution pattern To retailers in Lawrence, KS.
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[1760]
FDA event record
· Exact recall-number query on openFDA
