RecallHawk
Class II Recall

Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525

Albanese Confectionery Group, Inc.

Summary

The FDA issued a Class II for Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525 by Albanese Confectionery Group, Inc.. Reason: Product contains comingled Olly Sleep dietary supplement which may cause drowsiness.

Details

Source

Food Recall

External ID

F-0984-2021

Action Date

2021-09-22

Status

Terminated

Category

food

Product Description

Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525

Lot/Code Info: Lot: 1202011130

Quantity Affected: 226 cases (12 retail units per case)

Reason for Recall

Product contains comingled Olly Sleep dietary supplement which may cause drowsiness

Distribution

Distributors in OK and MI for further distribution to retail stores

Type: Voluntary: Firm initiated

Recall Initiated: 2021-08-18

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Albanese Confectionery Group, Inc. has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Albanese Confectionery Group, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Albanese Confectionery Group, Inc. have FDA actions?

Albanese Confectionery Group, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0984-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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