CLASS I Food recall · Reported 16 May 2018 · FDA Enforcement Report

Lean Pro 8 Cookies & Cream Tub recalled by Labrada Nutrition

Labrada Nutrition is recalling Lean Pro 8 Cookies & Cream Tub, distributed nationwide in the US. The recall was initiated on 24 Apr 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot# 083707; UPC# 710779113435
Quantity recalled132 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1393-2018
FDA event ID
79958
Recalling firm
Labrada Nutrition, Houston, TX
Classification
Class I
Status
Terminated
Recall initiated
24 Apr 2018
FDA classified
8 May 2018
Reported
16 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Egg
Product category
Cookies

Timeline

24 Apr 2018Recall initiated by company
8 May 2018Classified by FDA+14 days
16 May 2018Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared egg

Product as listed by the FDA

Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub

Where it was distributed

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

Nationwide

Questions about this recall

Why was it recalled?

Undeclared egg

Which lots are affected?

Lot# 083707; UPC# 710779113435

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 79958

This product is part of a recall event; the main page for the event is Lean Pro 8 Chocolate Tub and Lean Pro 8 Chocolate Tub recalled.

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