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Sundial Herbal Products

4 recall records in Beverages.

2020

4 records

Class IITerminatedRecall F-1441-2020

Product description

SUNDIAL PRINCESS ALMAZ Traditional ETHIOPIAN Organic SPICED TEA; "***Improves circulation***eliminates gas stomach griping & cramps. Relieves acid reflux, coughs, flu, hay fever, allergies, breaks up mucus and fights infection***" packaged in a breathable-type bag within a box.

Reason for recall

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

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Event ID
85882
Code info
Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
Product quantity
Unknown
Distribution pattern
NY
Voluntary / mandated
FDA Mandated
Initial firm notification
Letter
Product type
Food
Recalling firm location
3609 Boston Rd, N/A, Bronx, NY, United States
Recall initiation date
06/30/2020
Center classification date
09/15/2020
Termination date
10/26/2022
Class IITerminatedRecall F-1485-2020

Product description

"***PALO DE BRAZIL***BRASIL WOOD***great to reduce the sugar in the blood and removes gall stone from the kidneys***INSTRUCTIONS. put the wood in pure water and keep in the refrigerator then drink when thirsty***"

Reason for recall

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

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Event ID
85882
Code info
Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
Product quantity
Unknown
Distribution pattern
NY
Voluntary / mandated
FDA Mandated
Initial firm notification
Letter
Product type
Food
Recalling firm location
3609 Boston Rd, N/A, Bronx, NY, United States
Recall initiation date
06/30/2020
Center classification date
09/15/2020
Termination date
10/26/2022
Class IITerminatedRecall F-1499-2020

Product description

"AXUM ETHOIPIAN HONEY BEVERAGE***SUNDIAL HERBS***"

Reason for recall

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

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Event ID
85882
Code info
Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
Product quantity
Unknown
Distribution pattern
NY
Voluntary / mandated
FDA Mandated
Initial firm notification
Letter
Product type
Food
Recalling firm location
3609 Boston Rd, N/A, Bronx, NY, United States
Recall initiation date
06/30/2020
Center classification date
09/15/2020
Termination date
10/26/2022
Class IITerminatedRecall F-1507-2020

Product description

Ethiopian Coffee

Reason for recall

Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.

View full record
Event ID
85882
Code info
Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020.
Product quantity
Unknown
Distribution pattern
NY
Voluntary / mandated
FDA Mandated
Initial firm notification
Letter
Product type
Food
Recalling firm location
3609 Boston Rd, N/A, Bronx, NY, United States
Recall initiation date
06/30/2020
Center classification date
09/15/2020
Termination date
10/26/2022