RecallHawk
Class II Recall

Enrico Biscotti - Cranberry Pistachio Biscotti 8 ounce bags 6 bags per case

The Enrico Biscotti Company

Summary

The FDA issued a Class II for Enrico Biscotti - Cranberry Pistachio Biscotti 8 ounce bags 6 bags per case by The Enrico Biscotti Company. Reason: Undeclared soy.

Details

Source

Food Recall

External ID

F-1018-2021

Action Date

2021-10-06

Status

Terminated

Category

food

Product Description

Enrico Biscotti - Cranberry Pistachio Biscotti 8 ounce bags 6 bags per case

Lot/Code Info: All lots within shelf life

Quantity Affected: 3840 bags (total)

Reason for Recall

Undeclared soy

Distribution

Distributed to distributors in Ohio and New York.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-13

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 43 food recalls issued in the same week, part of 204 food-related FDA actions this month.

The Enrico Biscotti Company has 2 FDA actions in our database, including 2 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 (The Enrico Biscotti Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The Enrico Biscotti Company have FDA actions?

The Enrico Biscotti Company has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1018-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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