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Blue Tape Sriracha Recall: Acidified product was manufactured by firm without ODA license.

United States

TerminatedClass II

Company
Blue Tape Sriracha
Product
Blue Tape Sriracha sauce is refrigerated condiment, packaged…
Recall date
September 3, 2024
Terminated
December 13, 2024
Source
FDA

Reason for recall

Acidified product was manufactured by firm without ODA license.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Blue Tape Sriracha sauce is refrigerated condiment, packaged in a 10.5oz clear squeeze bottle, sold individually. Ingredients: Chilies, Garlic, Capsicum, Sugar, Salt, White Wine Vinegar. There is no company address on the label and no UPC code. Not published in this source record 136 bottles Best by date was marked on each bottle for 6 months from the date it was produced. No lot codes.

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0005-2025
Event ID
95298
Status
Terminated
Classification
Class II
Company
Blue Tape Sriracha
Product description
Blue Tape Sriracha sauce is refrigerated condiment, packaged in a 10.5oz clear squeeze bottle, sold individually. Ingredients: Chilies, Garlic, Capsicum, Sugar, Salt, White Wine Vinegar. There is no company address on the label and no UPC code.
Quantity
136 bottles
Reason
Acidified product was manufactured by firm without ODA license.
Recall initiation date
September 3, 2024
Report date
October 9, 2024
Classification date
Not published in this source record
Termination date
December 13, 2024
Distribution pattern
Nationwide
UPC, lot, and code information
Best by date was marked on each bottle for 6 months from the date it was produced. No lot codes.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Blue Tape Sriracha

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.