Gold Coast Packing Broccoli Florets recall
Recalled by Fresh Venture Foods, LLC · Santa Maria, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Firm test results found potential E-coli contamination in Broccoli Florets
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Gold Coast Packing Broccoli Florets; packed in the following configurations: 12 x 2 lb - Product code 508215 - Costco Canada; 1 x 40 lb.- Product code 504405 4 x 3 lb. - Product Codes 503401; 503409 4 x 3 lb. pizza cut -Product Code 503405 4 x 3 lb. - Mini florets - Product code 503412 2 x 5 lb. - Asian cut -Product code 505200; Distributed by Gold Coast Packing Co., Santa Maria, CA 93454
Quantity: 1204 total cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Use by Date: 8/12/17; 4 x 3 lb. 1.product code 503401: lot codes: 208 171053; 2. product code 503409; lot code 208 170812; 3. Pizza cut product code 503405; lot code 208 170976; 3. Mini Florets product code 503412, lot code 208 170976. 12 x 2 lb. Costco Canada, product code 508215; lot codes 208-170812, 208 171053. 2 x 5lb.; Asian cut product code 505200, lot 208 171053. 1x40 lb. Product code 504405, Lots 208 170976, 208 170996;
Where it was sold
California Colorado Minnesota Missouri North Carolina New York Ohio Oregon South Carolina
FDA's distribution note: California, Colorado, Minnesota, Missouri, North Carolina, New York, Ohio, Oregon, South Carolina and Canada
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Fresh Venture Foods, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 2, 2017
- In FDA report of
- Aug 30, 2017
- Terminated
- Nov 7, 2017
- FDA recall number
- F-3411-2017 · event 77879
- Official record
- FDA enforcement report search