Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS 4/24 BUNCH ITALIAN PARSLEY BAGS PRODUCE OF U.S.A. PACIFIC INT
Summary
The FDA issued a Class I for Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS 4/24 BUNCH ITALIAN PA by Pacific International Marketing. Reason: Potential contamination with Salmonella..
Details
Source
Food Recall
External ID
H-0177-2026
Action Date
2025-11-19
Status
Terminated
Category
food
Product Description
Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS 4/24 BUNCH ITALIAN PARSLEY BAGS PRODUCE OF U.S.A. PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 Carton Sticker Label: Conv Italian Parsley 4/24 CT Display Pacific Product of USA Distributed By: Dynasty Farms Salinas, CA 93905 UPC 40695 80120 Plastic Bag Label: ITALIAN PARSLEY CONTAINS 24 BUNCHES OF ITALIAN PARSLEY PRODUCE OF U.S.A. Distributed By: Pacific International Marketing P.O. Box 3737 Salinas, CA 93912 www.pim4u.com Plastic Bag Sticker Label: 25SAFPRIS56 Harvested On: 09 22 25 Twist Tie (for bunches) Label: FLAT PARSLEY PLU #4901 PROUDCT OF USA UPC 40695 80125
Lot/Code Info: Lot: 25SAFPRIS56
Quantity Affected: 160 cases (4 bags/case; 24 bunches/bag)
Reason for Recall
Potential contamination with Salmonella.
Distribution
AZ, CA, FL, GA, MN, MI, NV, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-27
Company
Salinas, 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 44 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Pacific International Marketing has 4 FDA actions in our database, including 4 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 (Pacific International Marketing) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pacific International Marketing have FDA actions?
Pacific International Marketing has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0177-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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