OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDI
Summary
The FDA issued a Class I for OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, by Fayus Inc.. Reason: Undeclared milk..
Details
Source
Food Recall
External ID
H-1329-2026
Action Date
2026-09-09
Status
Ongoing
Category
food
Product Description
OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDIENTS: Processed Dehydrated Yam Flour, freshness preserved by BHT & sodium bisulfite. UPCs: (2 lb): 650655244825, (4 lb): 650655496873, (5 lb): 650655244856, (10 lb): 650655244702 Manufacturer information is printed on the front label panel: Manufactured by: Yusol International Foods Sacramento CA 95828 www.yusolfood.com. The 10-lb bag is distributed to multiple consignees. The firm erroneously packed product for the Canadian consignee into the wrong bags printed and intended for the UK consignee, which had this manufacturing information printed on the front panel: U.K. Sole Distributor Funbel Ventures Ltd. Unit F7 Stephenson Close, Hoddesdon Hertfordshire EN11 OBW; www.funbelventures.net; info@funbelventures.net.
Lot/Code Info: All batch codes.
Quantity Affected: Unknown
Reason for Recall
Undeclared milk.
Distribution
Domestic: CA, GA, IL, NJ, NY, TX Foreign: Canada, Australia
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-06
Company
Sacramento, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 41 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Fayus Inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Fayus Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fayus Inc. have FDA actions?
Fayus 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 "H-1329-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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