Why it was recalled
Product contains undeclared milk.
Product description
ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1500 mg 325 tablets
Lot numbers, UPCs & expiration codes
Lot/Unit Numbers: 403122, 508080, 604166
Where it was sold
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 to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-1768-2016
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- May 20, 2016
- FDA report date
- Sep 21, 2016
- Quantity
- less than 1000 of all/lots products involved in this recall
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Ultimate Nutrition, Inc.
Original FDA data
Every field from FDA enforcement report F-1768-2016, exactly as published.
Show all FDA fields
- City
- Farmington
- State
- CT
- Status
- Terminated
- Country
- United States
- Event ID
- 74219
- Address
- 21 Hyde Rd
- Code information
- Lot/Unit Numbers: 403122, 508080, 604166
- Postal code
- 06032-2801
- Report date
- Sep 21, 2016
- Product type
- Food
- Recall number
- F-1768-2016
- Classification
- Class I
- Recalling firm
- Ultimate Nutrition, Inc.
- Product quantity
- less than 1000 of all/lots products involved in this recall
- Termination date
- Jul 27, 2017
- Reason for recall
- Product contains undeclared milk.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement 1500 mg 325 tablets
- Distribution pattern
- 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.
- Recall initiation date
- May 20, 2016
- Initial firm notification
- Press Release
- Center classification date
- Sep 13, 2016