Abee Med, 60 capsules per bottle. Manufactured by Sunset Natural Products
Check against the official notice below — it lists the full affected range.
Sunset Natural Products Inc. is recalling Abee Med dietary supplement (60 capsules per bottle) due to a consent decree issued by the FDA. The recall affects products manufactured or distributed since April 2, 2014. The recalled product was distributed in Florida and Nevada, with 3,149 bottles (totaling 240,000 capsules) affected. The specific lot involved is Lot #420415 with an expiration date of 04/18 and UPC 850993004017.
Under the terms of the consent decree, Sunset Natural Products Inc. and its owners are prohibited from marketing dietary supplements and must recall and destroy the affected products. The company must also hire a current Good Manufacturing Practice (cGMP) expert and obtain written permission from the FDA before resuming operations. The source document does not specify what actions affected consumers should take.
Written by software from the official notice below. Not reviewed by a lawyer.
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 manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Reason for recall: 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 manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations. Distribution: FL and NV Quantity: 3,149 bottles (240,000 caps) Lot/code info: Lot # 420415 Exp. Date 04/18 UPC 850993004017
Official record: FDA (Food enforcement) ↗
Republished from the official source above; details can change — the source record controls.