American Spoon¿ Sour Cherry PRESERVES Richer in Fruit
Reason American Spoon, Sour Cherry Preserves, 9.5 oz (UPC 019363010106) may contain mold.
American Spoon Food Sour Cherry Marmalade recall
Recalled by American Spoon Foods, Inc. · Petoskey, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product may have mold in jar.
Some molds produce toxins, and mold growth usually points to a problem with moisture, packaging or storage. All mold recalls.
What was recalled
American Spoon Food Sour Cherry Marmalade, 9.5 oz in glass jars with metal lid e. Total package size (e.g. 12 packages per case): 12 jars per case
Quantity: 682 jars
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.
Catalog #: MARM-CH, Lots:408400040001 - 408400040431, Best flavor date: 03/2016 and Lots: 408400050001 - 408400050459, Best flavor date: 03/2016
Where it was sold
Alabama Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Iowa Illinois Indiana Kansas Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina Nebraska New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Virginia Washington Wisconsin West Virginia
FDA's distribution note: AL, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI AND WV.
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
- American Spoon Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 21, 2014
- In FDA report of
- Aug 27, 2014
- Terminated
- Nov 14, 2014
- FDA recall number
- F-2343-2014 · event 68872
- Official record
- FDA enforcement report search