Jugos La Morove¿a, Parcha (Passion Fruit),Elaborado y Envasado por Jugos La Morove¿a…
Jugos y Agua La Morovena Inc. recalled this product and the FDA reported the enforcement action on 29 March 2017 as Class III. The recall was initiated by the firm. Juice product labels lack the statement "Phenylketonurics: Contains Phenylalanine"
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
Product
Jugos La Morove¿a, Parcha (Passion Fruit),Elaborado y Envasado por Jugos La Morove¿a, Carr 634 km 5.1, Bo. Franquez, Morovis PR 00687
Reason for recall
Juice product labels lack the statement "Phenylketonurics: Contains Phenylalanine"
Five things about this record are not in the record itself, and each one changes how it should be read.
Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
This is one of 9 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 9 separate recalls, which almost every published figure does, overstates it by a factor of 9. All 9 of them are listed on this page.
The recall ran for 20 months, from 17 February 2017 to termination on 15 October 2018. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
The FDA published the enforcement report 6 weeks after the firm began the recall.
The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Every product in this recall
The FDA opened 9 enforcement records for this one recall, one per product code. This page carries all of them; the 8 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.
