Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard b
Summary
The FDA issued a Class II for Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blu by Supherb Farms. Reason: Potential contamination with foreign objects..
Details
Source
Food Recall
External ID
F-0739-2025
Action Date
2025-04-30
Status
Completed
Category
food
Product Description
Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard box
Lot/Code Info: Lots: 003741 - 10.19.24; 003751 - 10.19.24; 003733 - 10.20.24; 003734 - 10.20.24; 003737 - 10.20.24; 003756 - 10.21.24; 003762 - 10.21.24
Quantity Affected: 96,000 lbs (3,200 cases - 30 lbs/case)
Reason for Recall
Potential contamination with foreign objects.
Distribution
United States: CA, MA, MI, NY, OH, OR, TX, WA; Canada; Mexico
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-03
Company
Turlock, CA
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 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Supherb Farms has 3 FDA actions in our database, including 3 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 (Supherb Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Supherb Farms have FDA actions?
Supherb Farms has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0739-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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