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Class III: unlikely to cause harmTerminated

Coca-Cola Consolidated Dr. Pepper Recall

Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Peppe…

Coca-Cola Consolidated · Charlotte, NC

Risk level
Class III
Reported by FDA
Feb 1, 2017
Recall ID
F-1344-2017
Check your lot numberHow we source this data

Summary

Coca-Cola Consolidated recalled Dr. Pepper starting Jan 5, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1344-2017 on Feb 1, 2017. Reason: Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener). Status: Terminated.

Why it was recalled

Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).

Product description

Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.

Lot numbers, UPCs & expiration codes

Date Code MAR2717syf

Where it was sold

NC

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-1344-2017
Classification
Class III
Status
Terminated
Recall initiated
Jan 5, 2017
FDA report date
Feb 1, 2017
Quantity
297 cases (8 bottles/case)
Recall type
Voluntary: Firm initiated
Recalling firm
Coca-Cola Consolidated

Original FDA data

Every field from FDA enforcement report F-1344-2017, exactly as published.

Show all FDA fields
City
Charlotte
State
NC
Status
Terminated
Country
United States
Event ID
76271
Address
4901 Chesapeake Dr
Code information
Date Code MAR2717syf
Postal code
28216-2905
Report date
Feb 1, 2017
Product type
Food
Recall number
F-1344-2017
Classification
Class III
Recalling firm
Coca-Cola Consolidated
Product quantity
297 cases (8 bottles/case)
Termination date
Jan 30, 2017
Reason for recall
Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).
Voluntary / mandated
Voluntary: Firm initiated
Product description
Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.
Distribution pattern
NC
Recall initiation date
Jan 5, 2017
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jan 25, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1344-2017, published Feb 1, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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