CLASS II ONGOING Drug recall · Reported 20 Nov 2024 · FDA Enforcement Report
30 day Supply recalled by Trinity Gold Nutrition
Trinity Gold Nutrition is recalling 30 day Supply, distributed nationwide in the US. The recall was initiated on 6 Nov 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0042-2025
- FDA event ID
- 95587
- Recalling firm
- Trinity Gold Nutrition, Fort Mill, SC
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 6 Nov 2024
- FDA classified
- 12 Nov 2024
- Reported
- 20 Nov 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
Timeline
| 6 Nov 2024 | Recall initiated by company | |
| 12 Nov 2024 | Classified by FDA | +6 days |
| 20 Nov 2024 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac and phenylbutazone.
Product as listed by the FDA
Trinity Gold Nutrition, 60 Capsule, 30 day Supply, Distributed by Trinity Gold Nutrition 201 Tom Hall St. Ste. 2107, Fortmill, SC 29716, USA, Ph: 704-629-8203, www.trinitygold.com, Made in India, UPC 802992001009
Where it was distributed
Nationwide within the United States; additionally Canada, England, and Australia.
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac and phenylbutazone.
Which lots are affected?
Lot #: IN-030, Exp. Date: NOV 2027
Where was it sold?
Nationwide within the United States; additionally Canada, England, and Australia.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.