Class IITerminated · reported 2015-04-01

Frozen vegetable-based burgers RETAIL - DOMESTIC: Organic Sunshine Burgers Gluten Free…

Sunshine Burger & Specialty Food Company, LLC recalled this product and the FDA reported the enforcement action on 1 April 2015 as Class II. The recall was initiated by the firm. Gluten testing was performed on products labeled gluten free. The results received back were >20ppm.

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
Frozen vegetable-based burgers RETAIL - DOMESTIC: Organic Sunshine Burgers Gluten Free Soy Free Vegan Barbecue 3 Organic Veggie Burgers Keep Frozen Net WT: 8 OZ. Best Before: 5/4/16; 6/11/2016; 8/13/16; CANADIAN: Organic Sunshine Burgers Barbecue 3 Organic Veggie Burgers Galettes Veggie biologiques Keep Frozen/Garder Congale 3-75 g Burgers/galettes 227 g Best Before/meilleur avant: 16/05/2016
Reason for recall
Gluten testing was performed on products labeled gluten free. The results received back were >20ppm.
Firm location
Bridgeville, Delaware, United States
Classification
Class II
Status
Terminated
Recall number
F-1614-2015
Quantity
4113 - 8 oz. packages
Distribution
CA CO IL MA NH NJ PA WA WI Canada
Initiated
27 February 2015
Reported by FDA
1 April 2015
Terminated
14 August 2015
Firm notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes
Retail: Item #000023 BBQ Flavor Best Before: 5/4/16, 6/11/2016, 8/13/16 Canadian: Item #010023 BBQ Flavor Best Before: 5/4/16

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 3 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 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. All 3 of them are listed on this page.
  • The recall ran for 6 months, from 27 February 2015 to termination on 14 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 5 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 3 enforcement records for this one recall, one per product code. This page carries all of them; the 2 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.

Other records from Sunshine Burger & Specialty Food Company, LLC

The FDA opens one enforcement record per product code, so several of these are frequently one recall event.

All 3 records for Sunshine Burger & Specialty Food Company, LLC

All 2015 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 access

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.