PlainRecalls
FDA Food Verify with FDA Food → Critical Class I Terminated

SPINACH FETA PIE (5 oz)

Reported: January 24, 2024 Initiated: December 5, 2023 #F-0717-2024 64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total) units

The recall

Nbrbdr Inc. dba Nutritious Delicious Foods issued this critical-severity FDA Food recall — Undeclared allergens; egg, milk, wheat.

Critical
severity level
64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total)
units affected
Class I
classification
January 24, 2024
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0717-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-0717-2024) was formally reported on January 24, 2024, with the manufacturer initiating the action on December 5, 2023. It is classified under Critical severity (Class I), with a current status of Terminated. Nbrbdr Inc. dba Nutritious Delicious Foods is listed as the recalling firm, operating out of South San Francisco, CA. Federal records indicate 64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total) units are affected, a scale large enough to require multi-state distribution tracking.

The documented reason for this recall is: Undeclared allergens; egg, milk, wheat Distribution data in the federal record shows the product reached: U.S. Distribution within the state of CA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Food. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 2 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Where this recall sits in the database

Severity2119858883High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified high severity.

Severity

Critical

Units Affected

64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total)

Related Recalls

6

6 from same agency

Product Description

SPINACH FETA PIE (5 oz)

Reason for Recall

Undeclared allergens; egg, milk, wheat

Details

Units Affected
64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total)
Distribution
U.S. Distribution within the state of CA
Location
South San Francisco, CA

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number F-0717-2024
Date reported January 24, 2024
Date initiated December 5, 2023
Recalling firm Nbrbdr Inc. dba Nutritious Delicious Foods
Units affected 64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total)
Distribution U.S. Distribution within the state of CA

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total) units affected — multi-state distribution scale.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units) ✓ This recall
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product was recalled?
SPINACH FETA PIE (5 oz). Recalled by Nbrbdr Inc. dba Nutritious Delicious Foods. Units affected: 64 PIES; 54 TRAYS OF 24 EACH SPANAKOPITA (Total).
Why was this product recalled?
Undeclared allergens; egg, milk, wheat
Which agency issued this recall?
This recall was issued by the FDA Food on January 24, 2024. Severity: Critical. Recall number: F-0717-2024.
Where was the recalled product distributed?
Distribution: U.S. Distribution within the state of CA.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-0717-2024) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as critical severity, meaning the product carries a reasonable probability of serious adverse health consequences or death. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Lowes Foods sour cream and onion flavored potato chips, 8oz… →

Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported January 24, 2024.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).