The Recall Desk
SevereFDA (Food)·F-0969-2017·Announced 2017-01-04

Sunset Natural Products Recalls Zinc Gluconate Capsules Under Consent Decree

Sunset Natural Products Inc. is recalling Zinc Gluconate 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, which aligns with the 'Severe' criteria for significant regulatory action and potential structural/quality defects.

Plain-English summary

Sunset Natural Products Inc. is recalling 1,540,000 capsules of Zinc Gluconate. 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 they recall and destroy all supplements manufactured or distributed since April 2, 2014, 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. Known lots include Lot # 130414 (Exp. 04/17), Lot # 261214 (Exp. 12/17), and Lot # 040815 (Exp. 08/18). The recall covers all dietary supplements manufactured, prepared, processed, packed, labeled, held, and/or distributed between April 2, 2014, and the date of the decree's entry.

Consumers who have these products should stop using them and follow the instructions provided in the consent decree to ensure they are destroyed under FDA supervision.

The recalled product

Product
Zinc Gluconate, bulk capsules
Manufacturer
Sunset Natural Products Inc.
Category
Food — Dietary Supplement
Hazard
Affected units
1,540,000

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 (13)

  • 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 # 130414 Exp. Date 04/17
  • Lot # 261214 Exp. Date 12/17
  • Lot # 040815 Exp. Date 08/18

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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