CLASS II Food recall · Reported 14 Mar 2018 · FDA Enforcement Report

Coca-Cola, Zero Sugar recalled by Heartland Coca-Cola Bottling

Heartland Coca-Cola Bottling is recalling Coca-Cola, Zero Sugar, distributed in Arkansas, Iowa, Illinois, Kansas, Missouri, Nebraska. The recall was initiated on 12 Feb 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes12 packs: May 14 18 LXD; 24 packs: Apr 30 18 LXC, May 14 18 LXB
Quantity recalled766,271 Cases Total

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-0900-2018
FDA event ID
79216
Recalling firm
Heartland Coca-Cola Bottling, Lenexa, KS
Classification
Class II
Status
Terminated
Recall initiated
12 Feb 2018
FDA classified
7 Mar 2018
Reported
14 Mar 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Soda

Timeline

12 Feb 2018Recall initiated by company
7 Mar 2018Classified by FDA+23 days
14 Mar 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

Sharp edges were observed on several of the cans which have the potential of causing cuts on the mouths of consumers who use the product.

Product as listed by the FDA

Coca-Cola, Zero Sugar, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Where it was distributed

Distributed to retail stores in AR, IA, IL, KS, MO, and NE.

ArkansasIowaIllinoisKansasMissouriNebraska

Questions about this recall

Is Coca-Cola, Zero Sugar recalled?

Yes. Heartland Coca-Cola Bottling recalled Coca-Cola, Zero Sugar on 12 Feb 2018. The recall is Class II and its status is Terminated. Recall number F-0900-2018.

Why was it recalled?

Sharp edges were observed on several of the cans which have the potential of causing cuts on the mouths of consumers who use the product.

Which lots are affected?

12 packs: May 14 18 LXD; 24 packs: Apr 30 18 LXC, May 14 18 LXB

Where was it sold?

Distributed to retail stores in AR, IA, IL, KS, MO, and NE.

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 21 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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