RecallHawk
Class II Recall

New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.)

Better Business...Better Foods, Inc.

Summary

The FDA issued a Class II for New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.) by Better Business...Better Foods, Inc.. Reason: Contains undeclared almonds & undeclared sesame.

Details

Source

Food Recall

External ID

F-0801-2025

Action Date

2025-05-21

Status

Ongoing

Category

food

Product Description

New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.)

Lot/Code Info: UPC (5 oz.): 609465693477 UPC (10 0z.): 642147152459 All codes recalled

Quantity Affected: 18,000 units

Reason for Recall

Contains undeclared almonds & undeclared sesame

Distribution

NY and New England

Type: Voluntary: Firm initiated

Recall Initiated: 2025-04-23

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

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 (Better Business...Better Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Better Business...Better Foods, Inc. have FDA actions?

This is the only FDA action we have on record for Better Business...Better Foods, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0801-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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