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4Patriots, LLC Recall: Milk not declared on product label.

United States

TerminatedClass II

Company
4Patriots, LLC
Product
4Patriots Chicken a la King CONTAINS: Wheat, Coconut NET W…
Recall date
November 15, 2018
Terminated
June 7, 2019
Source
FDA

Reason for recall

Milk not declared on product label.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
4Patriots Chicken a la King CONTAINS: Wheat, Coconut NET WT. 10.0 oz (284 g) Not published in this source record 5453 pouches lot# 18305006, lot# 18306006, lot# 1830906, lot# 1831006 Sold as a single unit in two separate kits (72 Hour Kit / 1 Week Kit, product numbers 72HK and 1WK)

Distribution

  • Distributed nationwide; product distributed exclusively by direct sale to customers.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0704-2019
Event ID
81590
Status
Terminated
Classification
Class II
Company
4Patriots, LLC
Product description
4Patriots Chicken a la King CONTAINS: Wheat, Coconut NET WT. 10.0 oz (284 g)
Quantity
5453 pouches
Reason
Milk not declared on product label.
Recall initiation date
November 15, 2018
Report date
December 19, 2018
Classification date
Not published in this source record
Termination date
June 7, 2019
Distribution pattern
Distributed nationwide; product distributed exclusively by direct sale to customers.
UPC, lot, and code information
lot# 18305006, lot# 18306006, lot# 1830906, lot# 1831006 Sold as a single unit in two separate kits (72 Hour Kit / 1 Week Kit, product numbers 72HK and 1WK)
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: 4Patriots, LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.