CLASS II Food recall · Reported 4 Jan 2017 · FDA Enforcement Report
Agma Care bulk) recalled by Sunset Natural Products
Sunset Natural Products is recalling Agma Care bulk), distributed in Florida, Nevada. The recall was initiated on 13 Oct 2015 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0923-2017
- FDA event ID
- 74054
- Recalling firm
- Sunset Natural Products, Miami, FL
- Brand
- Agma Care
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 13 Oct 2015
- FDA classified
- 28 Dec 2016
- Reported
- 4 Jan 2017
- Type
- FDA Mandated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Other
Timeline
| 13 Oct 2015 | Recall initiated by company | |
| 28 Dec 2016 | Classified by FDA | +442 days |
| 4 Jan 2017 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Product as listed by the FDA
Agma Care, (50,000 capsule bulk)
Where it was distributed
Products distributed to Florida, Nevada and the Dominican Republic
Questions about this recall
Is Agma Care bulk) recalled?
Yes. Sunset Natural Products recalled Agma Care bulk) on 13 Oct 2015. The recall is Class II and its status is Terminated. Recall number F-0923-2017.
Why was it 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.
Which lots are affected?
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 # 180515 Exp. Date 05/18
Where was it sold?
Products distributed to Florida, Nevada and the Dominican Republic
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Sunset Natural Products
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|---|---|---|---|---|---|
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