RecallHawk
Class II Recall

Brooklyn Delhi Ghost Pepper Hot Sauce, 5 oz., glass bottle

Brooklyn Delhi

Summary

The FDA issued a Class II for Brooklyn Delhi Ghost Pepper Hot Sauce, 5 oz., glass bottle by Brooklyn Delhi. Reason: Product may be become pressurized from fermentation and pose a safety risk to consumers who may sustain injuries to their eyes, face, and hands when o.

Details

Source

Food Recall

External ID

F-0918-2023

Action Date

2023-05-31

Status

Terminated

Category

food

Product Description

Brooklyn Delhi Ghost Pepper Hot Sauce, 5 oz., glass bottle

Lot/Code Info: UPC CODE: 85439008209 Best By: 12/12/2025 Batch #22121201 Best By: 12/13/2025 Batch #22121301 Best By: 1/3/2026 Batch #23010301 Best By:1/9/2026 Batch #23010901 Best By: 1/11/2026 Batch #23011101 Best By: 1/31/2026 Batch #23013101

Quantity Affected: 18,048 units

Reason for Recall

Product may be become pressurized from fermentation and pose a safety risk to consumers who may sustain injuries to their eyes, face, and hands when opening the bottles.

Distribution

1 Distributor in NY.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-27

Company

Brooklyn Delhi

Brooklyn, 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 71 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 (Brooklyn Delhi) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Brooklyn Delhi have FDA actions?

This is the only FDA action we have on record for Brooklyn Delhi in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0918-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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