The Recall Desk
SevereFDA (Food)·F-0971-2017·Announced 2017-01-04

Sunset Natural Products Recalls Aloe Vera Capsules Under Consent Decree

Sunset Natural Products Inc. is recalling Aloe Vera 500 mg bulk capsules pursuant to a consent decree requiring the destruction of supplements manufactured since April 2014.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class II, and the recall is mandated by a consent decree requiring the destruction of all products manufactured over a three-year period, indicating significant regulatory concerns regarding manufacturing practices.

Plain-English summary

Sunset Natural Products Inc. is recalling 12,310,000 capsules of Aloe Vera 500 mg bulk capsules. The recall is being conducted pursuant to a consent decree entered on September 25, 2015, which prohibits the company and its owners from marketing dietary supplements until specific corrective actions are completed.

The consent decree requires the firm to recall and destroy, under FDA supervision, all dietary supplements manufactured, prepared, processed, packed, labeled, held, and/or distributed between April 2, 2014, and the date of the decree's entry. The firm must also hire a cGMP expert and receive written permission from the FDA to resume operations.

The affected products were distributed to Florida, Nevada, and the Dominican Republic. Consumers should stop using the recalled capsules and follow the instructions provided by the recalling firm or the FDA regarding disposal or return.

The recalled product

Product
Aloe Vera 500 mg, bulk capsules
Manufacturer
Sunset Natural Products Inc.
Category
Food — Dietary Supplements
Hazard
Affected units
12,310,000

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • 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
  • 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

Distribution

Distributed in 2 states:

Part of a larger recall action

This product is one of 163 recalled by Sunset Natural Products Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 163 products in this recall →

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