Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs, NJ 07632…
Unilever United States, Inc. recalled this product and the FDA reported the enforcement action on 9 April 2014 as Class I. The recall was initiated by the firm. Unilever United States, Inc. is voluntarily recalling a limited number of 20-count boxes of Popsicle brand Orange, Cherry and Grape flavored ice pops because they may have been inadvertently exposed to milk, which is not listed as an ingredient on the label.
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
- Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs, NJ 07632 USA UPC 077567121301
- UPC
- 077567121301
- Reason for recall
- Unilever United States, Inc. is voluntarily recalling a limited number of 20-count boxes of Popsicle brand Orange, Cherry and Grape flavored ice pops because they may have been inadvertently exposed to milk, which is not listed as an ingredient on the label.
- Recalling firm
- Unilever United States, Inc.
- Firm location
- Englewood Cliffs, New Jersey, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1725-2014
- Quantity
- 17,922 cases approximately
- Distribution
- Nationwide
- Initiated
- 28 February 2014
- Reported by FDA
- 9 April 2014
- Terminated
- 11 August 2015
- Firm notified by
- Press Release
- Product codes
- best before dates of JUN0315GBV, JUN0415GBV, JUN0515GBV and JUN0615GBV
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. 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 record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 17 months, from 28 February 2014 to termination on 11 August 2015. 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.
- Recalls of ice cream or frozen dessert run a median of 7 months, so this one was longer than usual for its category. Ice cream and frozen desserts are ready to eat and never cooked again, and freezing preserves Listeria rather than killing it, which is why a positive environmental sample in a frozen dessert plant becomes a recall rather than a corrective action.
Filed under ice cream and frozen desserts and fresh produce. A product can sit in more than one.
Other ice cream and frozen desserts recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Unilever United States, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 5 other records name this firm.
All 6 records for Unilever United States, Inc.
All 2014 recalls · All FDA food recall data
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.
Early accessRecall 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.