Tastefully Simple Blackberry Syrup
Reason Presence of suspected mold in some units.
Product comes in as part of Fabulous Fudge Gift Box recall
Recalled by Tastefully Simple, Inc · Alexandria, MN, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Tastefully Simple is recalling various lots of Cookie & Cream Fudge(Fabulous Fudge Gift) because the product appears to have mold growing on the small chocolate cookie pieces on the top of the Cookies & Cream Fudge.
Some molds produce toxins, and mold growth usually points to a problem with moisture, packaging or storage. All mold recalls.
What was recalled
Product comes in as part of Fabulous Fudge Gift Box. The Gift box contains 2 samples of the recalled product, Cookies & Cream Fudge and 2 samples of a second product not being recalled. The product comes in small plastic container with lid (3.5" x 2.5" x 21.875"). A small spoon is also present in the package. Gift Box Label: Fabulous Fudge, Tastefully Simple, Cookies & Cream Fudge, Creamy Chocolate Fudge, 4 - 2.5 oz cups newt WT 10 oz (280 g), Item #421129. Individual Package Label: tastefully simple, Cookies & Cream Fudge, Net WT 2.5 oz (70 g), Item #758604.
Quantity: 4,257 gift sets and 1,638 indivdual units for a total of 10,152 units.
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.
Lot & (Best Buy Day): Lots: 3439 (02/09/15) , 3464 (02/09/15) , 3636 (02/09/15, 02/14/15, 02/15/15) , 3739 ( 02/14/15, 02/15/15, 04/13/15).
Where it was sold
Nationwide.
FDA's distribution note: Nationwide.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
- Tastefully Simple, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 18, 2014
- In FDA report of
- Dec 24, 2014
- Terminated
- Feb 4, 2015
- FDA recall number
- F-0713-2015 · event 69848
- Official record
- FDA enforcement report search