Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box distributed between 04/01/2026 and 06/
Summary
The FDA issued a Class II for Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a bo by Brooklyn Roasting Works LLC. Reason: Ambient storage of the product may lead to Clostridium botulinum toxin formation..
Details
Source
Food Recall
External ID
H-1179-2026
Action Date
2026-07-29
Status
Ongoing
Category
food
Product Description
Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box distributed between 04/01/2026 and 06/20/2026.
Lot/Code Info: Best By codes range: 063026 through 093026
Quantity Affected: 1219 units
Reason for Recall
Ambient storage of the product may lead to Clostridium botulinum toxin formation.
Distribution
NY and NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-02
Company
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 37 food recalls issued in the same week, part of 60 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 Roasting Works LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Brooklyn Roasting Works LLC have FDA actions?
This is the only FDA action we have on record for Brooklyn Roasting Works LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1179-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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