RecallHawk
Class II Recall

Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container Description: 4 x 9oz Bottles in Pack 24 unit

Betty Buzz LLC

Summary

The FDA issued a Class II for Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container Descr by Betty Buzz LLC. Reason: Beverage has off-odor.

Details

Source

Food Recall

External ID

F-0186-2023

Action Date

2022-12-14

Status

Terminated

Category

food

Product Description

Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container Description: 4 x 9oz Bottles in Pack 24 units per case

Lot/Code Info: Lot GF8.2 Best by 05/26/2023 UPC Codes: Bottle: 8-50029394129/ 4-Pack: 8-50029394136

Quantity Affected: 939 Cases/22,536 9oz Bottles

Reason for Recall

Beverage has off-odor

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-11-07

Company

Betty Buzz LLC

New York, NY

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 16 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 (Betty Buzz LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Betty Buzz LLC have FDA actions?

This is the only FDA action we have on record for Betty Buzz LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0186-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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