Brooklyn Delhi 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.
United States
TerminatedClass II
- Company
- Brooklyn Delhi
- Product
- Brooklyn Delhi Ghost Pepper Hot Sauce, 5 oz., glass bottle
- Recall date
- April 27, 2023
- Terminated
- December 8, 2023
- Source
- FDA
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Brooklyn Delhi Ghost Pepper Hot Sauce, 5 oz., glass bottle | Not published in this source record | 18,048 units | 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 |
Distribution
- 1 Distributor in NY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0918-2023
- Event ID
- 92241
- Status
- Terminated
- Classification
- Class II
- Company
- Brooklyn Delhi
- Product description
- Brooklyn Delhi Ghost Pepper Hot Sauce, 5 oz., glass bottle
- Quantity
- 18,048 units
- 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 opening the bottles.
- Recall initiation date
- April 27, 2023
- Report date
- May 31, 2023
- Classification date
- Not published in this source record
- Termination date
- December 8, 2023
- Distribution pattern
- 1 Distributor in NY.
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Brooklyn Delhi
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| New York | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
