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Sundial Herbal Products

46 recall records in Supplements.

2020

6 records

Class IITerminatedRecall F-1493-2020

Product description

"SUNDIAL***TRADITIONAL HERBAL FORMULA***ASTHMA***" packaged in boxes

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-1494-2020

Product description

"SUNDIAL***TRADITIONAL HERBAL FORMULA***BLOOD PRESSURE***" packaged in boxes

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-1495-2020

Product description

"SUNDIAL***TRADITIONAL HERBAL FORMULA***HEART***" packaged in boxes

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-1496-2020

Product description

"SUNDIAL***TRADITIONAL HERBAL FORMULA***Worms & Parasites***" packaged in boxes

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-1497-2020

Product description

"SUNDIAL***TRADITIONAL HERBAL FORMULA***Flu-Allergies HayFever***" packaged in boxes

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
Class IITerminatedRecall F-1498-2020

Product description

"SUNDIAL***TRADITIONAL HERBAL FORMULA***ARTHRITIS***" packaged in boxes

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