CLASS III Food recall · Reported 3 Oct 2018 · FDA Enforcement Report

Caffeine-Free Barq s Root Beer recalled by Swire Coca Cola U

Swire Coca Cola USA is recalling Caffeine-Free Barq s Root Beer, distributed nationwide in the US. The recall was initiated on 12 Sep 2018 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesMAY 2719 TOC MAY 2719 TOD
Quantity recalled2,945 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1988-2018
FDA event ID
81051
Recalling firm
Swire Coca Cola USA, West Valley City, UT
Classification
Class III
Status
Terminated
Recall initiated
12 Sep 2018
FDA classified
26 Sep 2018
Reported
3 Oct 2018
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Labeling Errors
Product category
Soda

Timeline

12 Sep 2018Recall initiated by company
26 Sep 2018Classified by FDA+14 days
3 Oct 2018Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Recalling Caffeine-Free Barq s Root Beer 12 Pack due to mislabeling.

Product as listed by the FDA

Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans

Where it was distributed

Nationwide. No govt/VA/military or foreign consignees.

Nationwide Virginia

Questions about this recall

Why was it recalled?

Recalling Caffeine-Free Barq s Root Beer 12 Pack due to mislabeling.

Which lots are affected?

MAY 2719 TOC MAY 2719 TOD

Where was it sold?

Nationwide. No govt/VA/military or foreign consignees.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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