Aloe Vera 500mg (Sunset Natural Products) – Regulatory Compliance (2015)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Aloe Vera 500 mg, bulk capsules
Brand
Sunset Natural Products Inc.
Lot Codes / Batch Numbers
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 lots and expiration dates: Lot # 170414 Exp. Date 05/17, Lot # 260414 Exp. Date 05/17, Lot # 270414 Exp. Date 05/17, Lot # 430414 Exp. Date 05/17, Lot # 440414 Exp. Date 07/17, Lot # 450414 Exp. Date 06/17, Lot # 170514 Exp. Date 06/17, Lot # 180514 Exp. Date 06/17, Lot # 340514 Exp. Date 08/17, Lot # 350514 Exp. Date 08/17, Lot # 360514 Exp. Date 09/17, Lot # 370514 Exp. Date 08/17, Lot # 050814 Exp. Date 09/17, Lot # 060814 Exp. Date 10/17, Lot # 070814 Exp. Date 10/17, Lot # 080814 Exp. Date 10/17, Lot # 030914 Exp. Date 10/17, Lot # 040914 Exp. Date 10/17, Lot # 050914 Exp. Date 10/17, Lot # 060914 Exp. Date 10/17, Lot # 190914 Exp. Date 09/17, Lot # 220914 Exp. Date 09/17, Lot # 240914 Exp. Date 09/17, Lot # 380914 Exp. Date 10/17, Lot # 390914 Exp. Date 11/17, Lot # 400914 Exp. Date 11/17, Lot # 410914 Exp. Date 11/17, Lot # 501014 Exp. Date 11/17, Lot # 511014 Exp. Date 11/17, Lot # 521014 Exp. Date 11/17, Lot # 531014 Exp. Date 11/17
Products Sold
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 lots and expiration dates: Lot # 170414 Exp. Date 05/17, Lot # 260414 Exp. Date 05/17, Lot # 270414 Exp. Date 05/17, Lot # 430414 Exp. Date 05/17, Lot # 440414 Exp. Date 07/17, Lot # 450414 Exp. Date 06/17, Lot # 170514 Exp. Date 06/17, Lot # 180514 Exp. Date 06/17, Lot # 340514 Exp. Date 08/17, Lot # 350514 Exp. Date 08/17, Lot # 360514 Exp. Date 09/17, Lot # 370514 Exp. Date 08/17, Lot # 050814 Exp. Date 09/17, Lot # 060814 Exp. Date 10/17, Lot # 070814 Exp. Date 10/17, Lot # 080814 Exp. Date 10/17, Lot # 030914 Exp. Date 10/17, Lot # 040914 Exp. Date 10/17, Lot # 050914 Exp. Date 10/17, Lot # 060914 Exp. Date 10/17, Lot # 190914 Exp. Date 09/17, Lot # 220914 Exp. Date 09/17, Lot # 240914 Exp. Date 09/17, Lot # 380914 Exp. Date 10/17, Lot # 390914 Exp. Date 11/17, Lot # 400914 Exp. Date 11/17, Lot # 410914 Exp. Date 11/17, Lot # 501014 Exp. Date 11/17, Lot # 511014 Exp. Date 11/17, Lot # 521014 Exp. Date 11/17, Lot # 531014 Exp. Date 11/17
Sunset Natural Products Inc. is recalling Aloe Vera 500 mg, bulk capsules due to Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and de. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, NV
Page updated: Jan 6, 2026