Class IITerminated in FDA datasetRecall initiated Sep 23, 2013

Martha White¿ Buttermilk Cornbread & Muffin Mix NET WT 6 OZ (170g) Laminated Pouch Mfg Code…

Recalling firm: J M Smucker Co

Why it was recalled

The states of Alabama and North Carolina through independent testing notified JM Smucker that aflatoxin levels exceeded FDA specification (<20 ppb). Levels tested ranged from 30…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 19, 2014.

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Compare the exact product and package details with the label you have.

ProductMartha White¿ Buttermilk Cornbread & Muffin Mix NET WT 6 OZ (170g) Laminated Pouch Mfg Code 3105 501 BEST IF USED BY: 15 APR 14 Product labeled in part INGREDIENTS: ENRICHED DEGERMINATED WHITE CORN MEAL, WHEAT FLOUR*** PARTIALLY DEHYDROGENATED SOYBEAN OIL, DEXTROSE, BAKING POWDER***MAY CONTAIN***DISTRIBUTED BY: MARTHA WHITE FOODS, INC. P.O. BOX 751030, MEMPHIS, TN 38175***0 13300 51701 7
Package size6 OZ

FDA code information

3105 501 BEST IF USED BY: 15 APR 14

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Full FDA record and distribution details

Original product description

Martha White¿ Buttermilk Cornbread & Muffin Mix NET WT 6 OZ (170g) Laminated Pouch Mfg Code 3105 501 BEST IF USED BY: 15 APR 14 Product labeled in part INGREDIENTS: ENRICHED DEGERMINATED WHITE CORN MEAL, WHEAT FLOUR*** PARTIALLY DEHYDROGENATED SOYBEAN OIL, DEXTROSE, BAKING POWDER***MAY CONTAIN***DISTRIBUTED BY: MARTHA WHITE FOODS, INC. P.O. BOX 751030, MEMPHIS, TN 38175***0 13300 51701 7

Original FDA recall reason

The states of Alabama and North Carolina through independent testing notified JM Smucker that aflatoxin levels exceeded FDA specification (<20 ppb). Levels tested ranged from 30 ppb to 207 ppb.

Recall details

Recall number
F-0107-2014
Event ID
66370
FDA status
Terminated
Initiated
Sep 23, 2013
Reported
Nov 13, 2013
Classified
Nov 4, 2013
Terminated
Jun 19, 2014
Quantity
10,906 cs/12/6 oz pouches
Location
Orrville, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Product was shipped to the following states: AL, AR, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, LA, MD, ME, MO, MS, NC, NE, NM, NY, NV, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI and WY.

FDA source record · F-0107-2014

Data updated September 16, 2026. View official FDA data ↗

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