Class IITerminatedVoluntary: Firm initiated

Pero Family Farms Food Company LLC: food recall F-0149-2025

Pero Family Farms Food Company LLC of Delray Beach, FL recalled Pero Family Farms Squash Sliced Zucchinni & Yellow Squash, Net Wt. 11oz (311g) Plastic Tray, 4 trays per carton,… Reason: Squash products potentially contaminated with Listeria monocytogenes. The FDA listed it as Class II in its Enforcement Report dated Dec 4, 2024; distribution: Florida, Illinois, Missouri, Virginia.

Record status as published: Terminated (terminated Jan 17, 2025). 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
Pero Family Farms Squash Sliced Zucchinni & Yellow Squash, Net Wt. 11oz (311g) Plastic Tray, 4 trays per carton, Microwavable Tray, Keep Refrigerated. UPC 874896009764
Product quantity
3149 cases
Reason for recall
Squash products potentially contaminated with Listeria monocytogenes.
Codes, lots and dates on the package
Lot # 346918 Expiration Date: 10/28/2024
Distribution pattern
Domestic distribution only: FL, MO, IL, VA
Recalling firm
Pero Family Farms Food Company LLC, Delray Beach, FL
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 firmNov 5, 2024
Classified by the FDANov 25, 2024
Published in the Enforcement ReportDec 4, 2024
TerminatedJan 17, 2025

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0149-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.