Why it was recalled
The firm received notification that the products were manufactured under insanitary conditions.
Product description
Product #4124: Caramel dip in plastic containers
Lot numbers, UPCs & expiration codes
All containers dated between June 2013 and August 2013.
Where it was sold
The affected product was distributed in the following states: AK, AR, AZ, CA, CT, GA, IA, ID, IN, MA, MT, PA, TX & WI. The affected product was also distributed to Canada.
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-0709-2014
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Sep 24, 2013
- FDA report date
- Dec 11, 2013
- Quantity
- 83 cases, with 4 containers per case
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Gold Medal Products
Original FDA data
Every field from FDA enforcement report F-0709-2014, exactly as published.
Show all FDA fields
- City
- Cincinnati
- State
- OH
- Status
- Terminated
- Country
- United States
- Event ID
- 66436
- Address
- 10700 Medallion Dr
- Code information
- All containers dated between June 2013 and August 2013.
- Postal code
- 45241-4807
- Report date
- Dec 11, 2013
- Product type
- Food
- Recall number
- F-0709-2014
- Classification
- Class II
- Recalling firm
- Gold Medal Products
- Product quantity
- 83 cases, with 4 containers per case
- Termination date
- Dec 24, 2013
- Reason for recall
- The firm received notification that the products were manufactured under insanitary conditions.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Product #4124: Caramel dip in plastic containers
- Distribution pattern
- The affected product was distributed in the following states: AK, AR, AZ, CA, CT, GA, IA, ID, IN, MA, MT, PA, TX & WI. The affected product was also distributed to Canada.
- Recall initiation date
- Sep 24, 2013
- Initial firm notification
- Telephone
- Center classification date
- Dec 4, 2013