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FDA recall record

Lean Pro 8 Vanilla 2,268g (5lb) Tub

Recall F-1391-2018Class ITerminatedApril 24, 2018

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 October 19, 2018. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Lean Pro 8 Vanilla 2,268g (5lb) Tub

Reason

Undeclared egg

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.

  • Lean Pro 8 Vanilla 2,268g (5lb) Tub

Code information listed by FDA

Lot# 073437, 073447, 073457, 073467, 073477; UPC # 710779112834

Distribution and firm information

Recalling firm listed by FDA: Labrada Nutrition, Inc

Firm location listed by FDA: Houston, TX, United States

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

Product quantity listed by FDA: 3517 units

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.