Class IIOngoingVoluntary: Firm initiated

Del Mar Food Products Corp.: food recall H-0110-2026

Del Mar Food Products Corp. of Watsonville, CA recalled ORGANIC IQF CHOPPED SPINACH 35 lbs. Net Weight Product is not ready to eat. For food safety, cook to an internal… Reason: Potential contamination with Listeria monocytogenes. The FDA listed it as Class II in its Enforcement Report dated Oct 29, 2025; distribution: Minnesota.

Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
ORGANIC IQF CHOPPED SPINACH 35 lbs. Net Weight Product is not ready to eat. For food safety, cook to an internal temperature of 165 degrees F as measured with a food thermometer. PACKED BY DEL MAR FOOD PRODUCTS CORP., WATSONVILLE, CA 95077, U.S.A. UPC: 1822V
Product quantity
966 cases (35 lbs/case)
Reason for recall
Potential contamination with Listeria monocytogenes.
Codes, lots and dates on the package
Lot: 250107A, 250107B, 250107C, 250107D, 2501071, 2501072, 2501073 Expiration: January 7, 2027
Distribution pattern
U.S. Distribution: MN
Recalling firm
Del Mar Food Products Corp., Watsonville, CA
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Letter

Dates

EventDate
Recall initiated by the firmOct 7, 2025
Classified by the FDAOct 21, 2025
Published in the Enforcement ReportOct 29, 2025

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0110-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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