Recall Number: F-0966-2017
Why was Pinateina recalled?
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Check out this page for guidance on what to do if you've consumed food from recall F-0966-2017 .
City: Miami
State: Florida
Country: United States
Classification: Class II
Classification Date: 2016-12-28
Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Product Description: Pinateina
Report Date: 2017-01-04
Product Type: Food
Company: Sunset Natural Products Inc.
Status: Terminated
Recall Number: F-0966-2017
Postal Code: 33155-4509
Recall Initiation Date: 2015-10-13
Recall End Date: 2017-04-10
Event ID: 74054
Distribution Pattern: Products distributed to Florida, Nevada and the Dominican Republic
Voluntary Or Mandated: FDA Mandated
Initial Firm Notification: Letter
Extra Info: As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lot and expiration date: Lot # 550315 Exp. Date 04/18
Product Quantity: 500 Bottles
Address: 7345 SW 45th St
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