CLASS II Food recall · Reported 14 Dec 2016 · FDA Enforcement Report

A&W Cream Soda, Caffeine Free recalled by Chesterman

Chesterman is recalling A&W Cream Soda, Caffeine Free, distributed in 9 states. The recall was initiated on 25 Oct 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNov0716PLE, Nov2116PLB, Dec1216PLC, Jan0217PLA
Quantity recalled1,010/24/20 fl oz/bottles/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-0675-2017
FDA event ID
75500
Recalling firm
Chesterman, Sioux City, IA
Classification
Class II
Status
Terminated
Recall initiated
25 Oct 2016
FDA classified
8 Dec 2016
Reported
14 Dec 2016
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Other Reasons
Product category
Soda

Timeline

25 Oct 2016Recall initiated by company
8 Dec 2016Classified by FDA+44 days
14 Dec 2016Published in enforcement report+6 days

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

Reason for recall

Product is labeled "caffeine free" but testing revealed the presence of caffeine.

Product as listed by the FDA

A&W Cream Soda, 20 FL OZ, Caffeine Free

Where it was distributed

Product was distributed to AR, CO, IA, KS, MN, NE, OK, SD, and TN

ArkansasColoradoIowaKansasMinnesotaNebraskaOklahomaSouth DakotaTennessee

Questions about this recall

Why was it recalled?

Product is labeled "caffeine free" but testing revealed the presence of caffeine.

Which lots are affected?

Nov0716PLE, Nov2116PLB, Dec1216PLC, Jan0217PLA

Where was it sold?

Product was distributed to AR, CO, IA, KS, MN, NE, OK, SD, and TN

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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