AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU BARAH USA, INC.; Soft Plum Aloo Bukahara 1/2 LB; *May Contai
Summary
The FDA issued a Class II for AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU BARAH USA, INC.; Sof by Global Commodities Inc. Reason: Product contains undeclared sulfites (4.66 mg/serving)..
Details
Source
Food Recall
External ID
F-0568-2025
Action Date
2025-02-26
Status
Ongoing
Category
food
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.
Lot/Code Info: Best Before December 2027
Quantity Affected: unknown
Reason for Recall
Product contains undeclared sulfites (4.66 mg/serving).
Distribution
VA, IL, NJ, GA, MD, NY, FL, MA, OR, MO, CO, OH, PA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-09
Company
Hicksville, 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 204 food-related FDA actions this month.
Global Commodities Inc has 2 FDA actions in our database, including 2 recalls.
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 (Global Commodities Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Global Commodities Inc have FDA actions?
Global Commodities Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0568-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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