GLOBAL COMMODITIES INC Recall: Product contains undeclared sulfites (4.66 mg/serving).

🇺🇸 United States

1. January 9, 2025 - Recall initiated
2. February 26, 2025 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0568-2025

Event ID

96187

Status

Ongoing

Classification

Class II

Company

GLOBAL COMMODITIES INC

Product description

AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU BARAH USA, INC.; Soft Plum Aloo Bukahara 1/2 LB; *May Contain Sulfites As preservatives; UPC 882475049186; packaged in clear plastic bags.

Quantity

unknown

Reason

Product contains undeclared sulfites (4.66 mg/serving).

Recall initiation date

January 9, 2025

Report date

February 26, 2025

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

VA, IL, NJ, GA, MD, NY, FL, MA, OR, MO, CO, OH, PA

UPC, lot, and code information

UPC 882475049186; Best Before December 2027

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

July 18, 2026 ET

Responsible company: GLOBAL COMMODITIES INC

Other recalls from GLOBAL COMMODITIES INC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Virginia	1
Illinois	1
New Jersey	1
Georgia	1
Maryland	1
New York	1
Florida	1
Massachusetts	1
Oregon	1
Missouri	1
Colorado	1
Ohio	1
Pennsylvania	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: July 18, 2026 ET

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 "Ongoing." 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.

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