FLAV-R-PAC IQF Chopped Spinach
Reason IQF frozen chopped Spinach is recalled due to detection of elevated level of Cadmium.
Frozen Sliced Carrots recall
Recalled by Norpac Foods, Inc. · Stayton, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Green shelled soybeans (Edamame) are potentially mixed in with sliced carrots.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Frozen Sliced Carrots, packaged in 2 lbs. bag, sold under Simplot Classic brand. The UPC is 0 71179 1846 3 1. The product is labeled in parts: "***SIMPLOT CLASSIC***Sliced Carrots***NET WT 32 OZ. (2 LBS)***INGREDIENTS: CARROTS***KEEP FROZEN UNTIL READY TO USE. IF THAWED. DO NOT REFREEZE***Preparation Instructions***DISTRIBUTED BY: JR SIMPLOT COMPANY***BOISE, IDAHO 83707***PRODUCT OF U.S.A***".
Quantity: 40 cases/ 12 packages/2 lbs.
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.
BEST BY SEP 2015/ 5M3 13X2L4 HH:MM. Product has Best By SEPTEMBER 2015. The code 5M3 13X2L4 HH:MM meant the product was repacked into Poly Bags on September 13, 2013, 07:47 am to 14:32 pm at NORPAC Foods, Inc., Quincy Foods, LLC Plant 2, 222 Columbia Way, PO Box 127, Quincy, WA 98848.
Where it was sold
Illinois Missouri Nebraska
FDA's distribution note: Products distributed in Illinois, Missouri, and Nebraska.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Norpac Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 20, 2013
- In FDA report of
- Oct 30, 2013
- Terminated
- Jun 24, 2015
- FDA recall number
- F-0081-2014 · event 66375
- Official record
- FDA enforcement report search