Food recall: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1500 mg 325 tablets
Class I FDA enforcement event 74219. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Product contains undeclared milk.
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Ultimate Nutrition, Inc. started this food recall on 20 May 2016. The firm address in the FDA record is in Farmington, CT. FDA put the recall in Class I. FDA event 74219 has 3 product records. The first FDA enforcement report date is 21 Sep 2016. The record gives the status Terminated, with the termination date 27 Jul 2017.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
The recalled Amino Gold was distributed nationwide through distributors, stores, and web sites. The product was sold direct to distributors in CA, NC, ID, PA, CT.
Recalling firm
Ultimate Nutrition, Inc., Farmington, CT.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
3 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1768-2016 | ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1500 mg 325 tablets | less than 1000 of all/lots products involved in this recall | Class I | Terminated | 21 Sep 2016 |
| F-1769-2016 | ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1000 mg 250 capsules; UPC: 099071 00120 7 | less than 1000 of all/lots products involved in this recall | Class I | Terminated | 21 Sep 2016 |
| F-1770-2016 | ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement, 1000 mg, 250 tablets; UPC: 0 99071 00140 5 | less than 1000 of all/lots products involved in this recall | Class I | Terminated | 21 Sep 2016 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2016
- 799
- Share of these events in Class I
- 52%
- Product records in this event
- 3
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-1768-2016The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 74219. https://recallregister.com/fda/i/74219/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
The recalled Amino Gold was distributed nationwide through distributors, stores, and web sites. The product was sold direct to distributors in CA, NC, ID, PA, CT.
- What quantity of product is in FDA event 74219?
- The event has 3 product records. The first record gives this quantity:
less than 1000 of all/lots products involved in this recall
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2016 have the same class?
- 52% of the 799 food events that started in 2016 are in Class I.