FDA recall record
SPINACH FETA PIE (5 oz)
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of January 24, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
SPINACH FETA PIE (5 oz)
Reason
Undeclared allergens; egg, milk, wheat
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
SPINACH FETA PIE (5 oz)
Code information listed by FDA
All batch numbers BEST BUY NOVEMBER 17, 2023; NOVEMBER 24,2023; DECEMBER 1, 2023; DECEMBER 15, 2023
Distribution and firm information
Recalling firm listed by FDA: NBRBDR Inc. dba Nutritious Delicious Foods
Firm location listed by FDA: South San Francisco, CA, United States
Distribution reported by FDA: U.S. Distribution within the state of CA
Product quantity listed by FDA: 64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.