CLASS II Food recall · Reported 18 Mar 2026 · FDA Enforcement Report

Coco's Italian Market Cannoli Making Kit recalled

Cocos Wholesale and Imports is recalling Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, distributed in Tennessee. The recall was initiated on 3 Feb 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduct Number: 9927816; all lot codes within shelf life
Quantity recalled11 retail units

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
H-0554-2026
FDA event ID
98406
Recalling firm
Cocos Wholesale and Imports, Nashville, TN
Brand
Coco's
Classification
Class II
Status
Completed
Recall initiated
3 Feb 2026
FDA classified
11 Mar 2026
Reported
18 Mar 2026
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Ready Meals

Timeline

3 Feb 2026Recall initiated by company
11 Mar 2026Classified by FDA+36 days
18 Mar 2026Published 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

Label lists flour as a sub-ingredient of the shells, and ricotta cheese as a sub-ingredient of the cream but does not declare wheat or milk.

Product as listed by the FDA

Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt. 8 oz. (227g), Keep Frozen, packaged in a plastic container, UPC 0680334992716

Where it was distributed

TN

Tennessee

Questions about this recall

Why was it recalled?

Label lists flour as a sub-ingredient of the shells, and ricotta cheese as a sub-ingredient of the cream but does not declare wheat or milk.

Which lots are affected?

Product Number: 9927816; all lot codes within shelf life

Where was it sold?

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.

Other products in this recall event

1 other product · FDA event 98406

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