Why it was recalled
Product is labeled "caffeine free" but testing revealed the presence of caffeine.
Product description
A&W Cream Soda, 20 FL OZ, Caffeine Free
Lot numbers, UPCs & expiration codes
Nov0716PLE, Nov2116PLB, Dec1216PLC, Jan0217PLA
Where it was sold
Product was distributed to AR, CO, IA, KS, MN, NE, OK, SD, and TN
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-0675-2017
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 25, 2016
- FDA report date
- Dec 14, 2016
- Quantity
- 1,010/24/20 fl oz/bottles/cases
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Chesterman Co
Original FDA data
Every field from FDA enforcement report F-0675-2017, exactly as published.
Show all FDA fields
- City
- Sioux City
- State
- IA
- Status
- Terminated
- Country
- United States
- Event ID
- 75500
- Address
- 4700 S Lewis Blvd
- Code information
- Nov0716PLE, Nov2116PLB, Dec1216PLC, Jan0217PLA
- Postal code
- 51106-9516
- Report date
- Dec 14, 2016
- Product type
- Food
- Recall number
- F-0675-2017
- Classification
- Class II
- Recalling firm
- Chesterman Co
- Product quantity
- 1,010/24/20 fl oz/bottles/cases
- Termination date
- Mar 8, 2017
- Reason for recall
- Product is labeled "caffeine free" but testing revealed the presence of caffeine.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- A&W Cream Soda, 20 FL OZ, Caffeine Free
- Distribution pattern
- Product was distributed to AR, CO, IA, KS, MN, NE, OK, SD, and TN
- Recall initiation date
- Oct 25, 2016
- Initial firm notification
- Visit
- Center classification date
- Dec 8, 2016