PlainRecalls
FDA Food Verify with FDA Food → Critical Class I Terminated

ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement, 1000 mg, 250 tablets; UPC: 0 99071 00140 5

Reported: September 21, 2016 Initiated: May 20, 2016 #F-1770-2016 less than 1000 of all/lots products involved in this recall units

Ultimate Nutrition, Inc. issued this FDA Food recall on September 21, 2016. Classified as Critical severity (Class I). Approximately less than 1000 of all/lots products involved in this recall units are affected. The recall was issued because: Product contains undeclared milk.. This recall notice is sourced from official FDA Food enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This FDA Food action (record #F-1770-2016) was formally reported on September 21, 2016, with the manufacturer initiating the action on May 20, 2016. It is classified under Critical severity (Class I), with a current status of Terminated. Ultimate Nutrition, Inc. is listed as the recalling firm, operating out of Farmington, CT. Federal records indicate less than 1000 of all/lots products involved in this recall units are affected.

The documented reason for this recall is: Product contains undeclared milk. Distribution data in the federal record shows the product reached: 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.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Food. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Critical

Units Affected

less than 1000 of all/lots products involved in this recall

Related Recalls

6

6 from same agency

Product Description

ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement, 1000 mg, 250 tablets; UPC: 0 99071 00140 5

Reason for Recall

Product contains undeclared milk.

Details

Recalling Firm
Ultimate Nutrition, Inc.
Units Affected
less than 1000 of all/lots products involved in this recall
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.
Location
Farmington, CT

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number F-1770-2016
Date reported September 21, 2016
Date initiated May 20, 2016
Recalling firm Ultimate Nutrition, Inc.
Units affected less than 1000 of all/lots products involved in this recall
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.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

less than 1000 of all/lots products involved in this recall units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product was recalled?
ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement, 1000 mg, 250 tablets; UPC: 0 99071 00140 5. Recalled by Ultimate Nutrition, Inc.. Units affected: less than 1000 of all/lots products involved in this recall.
Why was this product recalled?
Product contains undeclared milk.
Which agency issued this recall?
This recall was issued by the FDA Food on September 21, 2016. Severity: Critical. Recall number: F-1770-2016.
Where was the recalled product distributed?
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..
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1770-2016) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as critical severity, meaning the product carries a reasonable probability of serious adverse health consequences or death. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).