CLASS II Food recall · Reported 27 Dec 2017 · FDA Enforcement Report

Sensations cinnamon roll Uncooked Dough recalled

AMS is recalling Sensations cinnamon roll Uncooked Dough. The recall was initiated on 8 Dec 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot/Unit Numbers: 18AL27
Quantity recalled37 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-0503-2018
FDA event ID
78726
Recalling firm
AMS, Bath, ME
Classification
Class II
Status
Terminated
Recall initiated
8 Dec 2017
FDA classified
18 Dec 2017
Reported
27 Dec 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Tree Nuts
Product category
Bread

Timeline

8 Dec 2017Recall initiated by company
18 Dec 2017Classified by FDA+10 days
27 Dec 2017Published in enforcement report+9 days

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

Reason for recall

Product contains undeclared pecans. Pecans are clearly visible to the consumer.

Product as listed by the FDA

Sensations cinnamon roll UNCOOKED DOUGH 450g, UPC: 236821197

Where it was distributed

Canada only.

Questions about this recall

Is Sensations cinnamon roll Uncooked Dough recalled?

Yes. AMS recalled Sensations cinnamon roll Uncooked Dough on 8 Dec 2017. The recall is Class II and its status is Terminated. Recall number F-0503-2018.

Why was it recalled?

Product contains undeclared pecans. Pecans are clearly visible to the consumer.

Which lots are affected?

Lot/Unit Numbers: 18AL27

Where was it sold?

Canada only.

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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