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Labrada Nutrition, Inc Recall: Undeclared egg

United States

TerminatedClass I

Company
Labrada Nutrition, Inc
Product
Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub
Recall date
April 24, 2018
Terminated
October 19, 2018
Source
FDA

Reason for recall

Undeclared egg

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub Not published in this source record 132 units Lot# 083707; UPC# 710779113435

Distribution

  • Distributed nationwide throughout the US and the following countries - Vietnam
  • Dom Republic
  • Kuwait
  • Panama
  • Saudi
  • Korea
  • Germany
  • Iceland
  • EU
  • Bermuda
  • Australia
  • Jordan

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1393-2018
Event ID
79958
Status
Terminated
Classification
Class I
Company
Labrada Nutrition, Inc
Product description
Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub
Quantity
132 units
Reason
Undeclared egg
Recall initiation date
April 24, 2018
Report date
May 16, 2018
Classification date
Not published in this source record
Termination date
October 19, 2018
Distribution pattern
Distributed nationwide throughout the US and the following countries - Vietnam, Dom Republic, Kuwait, Panama, Saudi, Korea, Germany, Iceland, EU, Bermuda, Australia, Jordan
UPC, lot, and code information
Lot# 083707; UPC# 710779113435
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 79958 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocola…
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Vanilla 2,268g (5lb) Tub
Published
May 16, 2018
Distribution
Nationwide

View recall →

Responsible company: Labrada Nutrition, Inc

Other recalls from Labrada Nutrition, Inc

FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocola…
Published
May 16, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Vanilla 2,268g (5lb) Tub
Published
May 16, 2018
Distribution
Nationwide

View recall →

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.