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U.B.C. Food Distributors INC. Recall: Potential Salmonella contamination

United States

TerminatedClass I

Company
U.B.C. Food Distributors INC.
Product
Baraka brand ground black pepper packaged in 7oz retail cont…
Recall date
May 28, 2024
Terminated
August 8, 2024
Source
FDA

Reason for recall

Potential Salmonella contamination

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Baraka brand ground black pepper packaged in 7oz retail containers with UPC 8 22514 26626 6; 10 units per case Not published in this source record 1070 units Best Before January 2026

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1345-2024
Event ID
94725
Status
Terminated
Classification
Class I
Company
U.B.C. Food Distributors INC.
Product description
Baraka brand ground black pepper packaged in 7oz retail containers with UPC 8 22514 26626 6; 10 units per case
Quantity
1070 units
Reason
Potential Salmonella contamination
Recall initiation date
May 28, 2024
Report date
June 19, 2024
Classification date
Not published in this source record
Termination date
August 8, 2024
Distribution pattern
Nationwide
UPC, lot, and code information
Best Before January 2026
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: U.B.C. Food Distributors INC.

Other recalls from U.B.C. Food Distributors INC.

FDA Recall United States Terminated Historical recordClass I

U.B.C. Food Distributors INC.

Product
Baraka Mild Curry Powder packed in 7 oz. Plastic Jar
Published
December 19, 2018
Distribution
Domestic: CO, IL, IN, MI, MO, MN, NE, NY…

View recall →

FDA Recall United States Terminated Historical recordClass I

U.B.C. Food Distributors INC.

Product
Baraka Hot Curry Powder packed in 7 OZ Plastic Jar
Published
December 19, 2018
Distribution
Domestic: CO, IL, IN, MI, MO, MN, NE, NY…

View recall →

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.