Kale, Apple & Greekstyle Yogurt Flexible pouch with Resealable spout. Packaged for…
Plum Inc recalled this product and the FDA reported the enforcement action on 4 December 2013 as Class II. The recall was initiated by the firm. Manufacturing defect leading to post-process contamination.
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
- Kale, Apple & Greekstyle Yogurt Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST COLLECTIVE, INC. EMERYVILLE, CA 94608 1-877-914-PLUM WWW.NEST-COLLECTIVE.COM
- Reason for recall
- Manufacturing defect leading to post-process contamination.
- Recalling firm
- Plum Inc
- Firm location
- Emeryville, California, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0380-2014
- Quantity
- 597,827 total cases, all varieties
- Distribution
- Nationwide and to Korea, China, Mexico, Hong Kong, Singapore, Malaysia, Costa Rica, jordan, Bermuda, Indonesia and United Kingdom
- Initiated
- 8 November 2013
- Reported by FDA
- 4 December 2013
- Terminated
- 4 March 2015
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- UK Export only Item number KAG11U; Selling Unit UPC; 5060116891621 Case UPC:5060116897777 Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. 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 30 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 30 separate recalls, which almost every published figure does, overstates it by a factor of 30. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 30 of them.
- The recall ran for 16 months, from 8 November 2013 to termination on 4 March 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 4 weeks after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was longer than usual for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Filed under milk and dairy and fresh produce. A product can sit in more than one.
Other milk and dairy 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 Plum Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 39 other records name this firm.
All 2013 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.