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FDA FOOD RECALLS

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Every FDA food recall since 2012, in one place. We check each recall's status with FDA every day.

Checked with FDA daily · Source: U.S. Food and Drug Administration

7,366 ended recalls · showing 2,941 to 2,960

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  1. ENDEDClass III · Low riskRecalled Jul 17, 2018

    Ranch Flavored Hazelnuts in 4 oz Round Type, in plastic bag, UPC 7 39059 20414 4 . Ranch Flavored H...

    Ranch Flavored Hazelnuts product is recalled due to undeclared hazelnut in the Contains statement.

    Holmquist Hazelnut Orchards · Lynden, WA

    Where it was sold: distributed in WA and sold on company website https://www.holmquisthazelnuts.com.

    UPC 739059204144UPC 739059206148UPC 739059216147
    Show details
    Product, as FDA describes it
    Ranch Flavored Hazelnuts in 4 oz Round Type, in plastic bag, UPC 7 39059 20414 4 . Ranch Flavored Hazelnuts in 6 oz Round Type, in plastic bag, UPC 7 39059 20614 8. Ranch Flavored Hazelnuts in 1 lb Round Type, in plastic bag, UPC 7 39059 21614 7. The product label is read in parts: "***Ranch Flavored Hazelnuts ***Ingrdients: Dry Roasted Hazelnuts, Vegetable Oil, Salt, Buttermilk Powder, Onion Powder, Garlic Powder, Dextrose, Black Pepper, Disodium Inosinate, and less than 2% Tricalcium Phosphate added to prevent caking. (Contains Milk)***".
    Reason, in FDA's words
    Ranch Flavored Hazelnuts product is recalled due to undeclared hazelnut in the Contains statement.
    Codes on the package
    Product is coded, but lot numbers are not tracked when distributed The affected lot # of 16 oz. (1 lb): 3E15J11957 3E15J12017 1E15Y12217 The affected lot # of 6 oz: 3E15J12017 1E15Y12217 241173317 3E1700937 003181078 The affected lot # 4 oz. 3E15J12017 2401733407 24243527 T17J10188 T16J10228
    Where it was sold
    distributed in WA and sold on company website https://www.holmquisthazelnuts.com.
    Amount recalled
    Total Ranch Hazelnuts = 1388 pkg.
    Status
    Ended Sep 28, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1725-2018
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Jul 17, 2018

    Seattle Sourdough Pub Buns 6 pack, net wt. 16 oz., UPC 0-72220-10164-5

    Seattle Sourdough Pub Buns 6 pack are recalled because it may contain undeclared SOY.

    Portland French Bakery L T D · Portland, OR

    Where it was sold: distributed in Alaska, California, Idaho, Montana, Oregon, Utah, Washington, and Wyoming.

    UPC 072220101645
    Show details
    Product, as FDA describes it
    Seattle Sourdough Pub Buns 6 pack, net wt. 16 oz., UPC 0-72220-10164-5
    Reason, in FDA's words
    Seattle Sourdough Pub Buns 6 pack are recalled because it may contain undeclared SOY.
    Codes on the package
    best before date between JUL- 03-18 and JUL-31-18.
    Where it was sold
    distributed in Alaska, California, Idaho, Montana, Oregon, Utah, Washington, and Wyoming.
    Amount recalled
    26,635 units
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1829-2018
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Jul 17, 2018

    Franz Premium Pub Buns 12 pack, net wt. 32 oz., UPC 0-72220-70218-7

    Franz Premium Pub Buns 12 pack are recalled because it may contain undeclared SOY.

    Portland French Bakery L T D · Portland, OR

    Where it was sold: distributed in Alaska, California, Idaho, Montana, Oregon, Utah, Washington, and Wyoming.

    UPC 072220702187
    Show details
    Product, as FDA describes it
    Franz Premium Pub Buns 12 pack, net wt. 32 oz., UPC 0-72220-70218-7
    Reason, in FDA's words
    Franz Premium Pub Buns 12 pack are recalled because it may contain undeclared SOY.
    Codes on the package
    best before date between JUL- 03-18 and JUL-31-18.
    Where it was sold
    distributed in Alaska, California, Idaho, Montana, Oregon, Utah, Washington, and Wyoming.
    Amount recalled
    8,022 units
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1830-2018
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Jul 14, 2018

    utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 173...

    Utz¿ Quality Foods, LLC., is voluntarily recalling select expiration dates of Utz¿ Carolina Style Barbeque Potato Chips due to undeclared soy allerge...

    Utz Quality Food Inc · Hanover, PA

    Where it was sold: AL, AR, CO, CT, DC, DE, FL, GA, IL, IN, KY, LA, MA, MD, ME, MS, NC, NE, NH, NJ, NY, OH, PA RI, SC, TN, TX, UT, VA, VT, WV

    UPC 041780001535UPC 041780000491
    Show details
    Product, as FDA describes it
    utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC: 0-41780-00153-5; utz Carolina Style Barbeque Potato Chips, Net Wt 7.5 OZ; UTZ Quality Foods, LLV, Hanover, PA 17301; UPC: 0-41780-00049-1
    Reason, in FDA's words
    Utz¿ Quality Foods, LLC., is voluntarily recalling select expiration dates of Utz¿ Carolina Style Barbeque Potato Chips due to undeclared soy allergen.
    Codes on the package
    Utz 2.875 oz., UPC: 0-41780-00153-5, Exp date range: October 6th to October 20th. Utz 7.5 oz. , UPC: 0-41780-00049-1, EXp date range: August 18th to October 27th.
    Where it was sold
    AL, AR, CO, CT, DC, DE, FL, GA, IL, IN, KY, LA, MA, MD, ME, MS, NC, NE, NH, NJ, NY, OH, PA RI, SC, TN, TX, UT, VA, VT, WV
    Amount recalled
    96,278 total bags
    Status
    Ended Nov 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1753-2018
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Jul 12, 2018

    Kowalski's Markets kalbi rub. Net Wt 5.5 oz. (155.9 g), UPC 79147-00243. Distributed by: Kowalski...

    An ingredient contains wheat, which is not declared on the label.

    J and J Bunting, Inc · Rogers, MN

    Where it was sold: MN

    UPC 079147002437
    Show details
    Product, as FDA describes it
    Kowalski's Markets kalbi rub. Net Wt 5.5 oz. (155.9 g), UPC 79147-00243. Distributed by: Kowalski's Markets, Woodbury, MN 55125
    Reason, in FDA's words
    An ingredient contains wheat, which is not declared on the label.
    Codes on the package
    K587, L386, L470, M12, M345
    Where it was sold
    MN
    Amount recalled
    117 cases (12 glass jars per case)
    Status
    Ended Jul 26, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1661-2018
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Jul 12, 2018

    Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ (340g)***THIS SIDE UP IN MICROWAVE*...

    Undeclared allergens on the labeling.

    The Pictsweet Company · Bells, TN

    Where it was sold: Product was distributed in the following states: CA, GA, IL, MD, NC, TX and VA.

    Show details
    Product, as FDA describes it
    Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ (340g)***THIS SIDE UP IN MICROWAVE***Nutrition Facts***INGREDIENTS: BRUSSEL SPROUTS***
    Reason, in FDA's words
    Undeclared allergens on the labeling.
    Codes on the package
    1508KC, 1508KD and 1508KE; BEST IF USED BY MAY 30 2020
    Where it was sold
    Product was distributed in the following states: CA, GA, IL, MD, NC, TX and VA.
    Amount recalled
    960 Cases/ 7 Bags per case
    Status
    Ended Nov 2, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1770-2018
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Jul 10, 2018

    Lenny's Maryland Crab Mix

    Undeclared wheat on the product label

    Lenni's Crab Mix, Inc · Destin, FL

    Sold in the U.S. (states not listed)

    Where it was sold: US Consignees only. (3) consignees only.

    Show details
    Product, as FDA describes it
    Lenny's Maryland Crab Mix
    Reason, in FDA's words
    Undeclared wheat on the product label
    Codes on the package
    TBD
    Where it was sold
    US Consignees only. (3) consignees only.
    Amount recalled
    408 cases (128oz) 1 gallon
    Status
    Ended Oct 9, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1964-2018
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Jul 2, 2018

    Naked Bread Hamburger Buns #NothingToHide, 8 pack. Product is packaged in low density polyethylene ...

    Naked Bread Hamburger Buns #NothingToHide, 8 pack, are recalled due to undeclared milk.

    United States Bakery Corp · Portland, OR

    Where it was sold: distributed directly in California, Idaho, Montana, Oregon, Utah, Washington

    UPC 072220110753
    Show details
    Product, as FDA describes it
    Naked Bread Hamburger Buns #NothingToHide, 8 pack. Product is packaged in low density polyethylene bag and identified as Naked Bread Hamburger Buns #NothingToHide, Net wt. 16.5 oz., UPC #72220 11075. The label is read in parts: "***INGREDIENTS: ENRICHED UNBLEACHED WHEAT FLOUR (WHEAT FLOUR, MALTED BARLEY FLOUR, NIACIN, REDUCED IRON, THIAMIN MONONITRATE, RIBOFLAVIN AND FOLIC ACID(, WATER, YEAST, SUGAR, VITAL WHEAT GLUTEN, PALM OIL*** CONTAINS: WHEAT***".
    Reason, in FDA's words
    Naked Bread Hamburger Buns #NothingToHide, 8 pack, are recalled due to undeclared milk.
    Codes on the package
    F6 Best By June 16th, 2018 through July 16th 2018. F6 is location
    Where it was sold
    distributed directly in California, Idaho, Montana, Oregon, Utah, Washington
    Amount recalled
    22,459 bags
    Status
    Ended Sep 20, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1663-2018
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Jun 29, 2018

    Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 6...

    The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.

    LL'S MAGNETIC CLAY INC · Austin, TX

    Where it was sold: Nationwide throughout the United States and United Kingdom, Mexico, Netherlands, Sweden, Australia, Canada, Hong Kong, Spain, New Zealand, Chile, Taiwan, Switzerland, Albania, Pola...

    UPC 853956003157UPC 853956003539
    Show details
    Product, as FDA describes it
    Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
    Reason, in FDA's words
    The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
    Codes on the package
    All Lots within expiry; Lot # s: 1356300 (exp. 01/2019), 1405700 (exp. 03/2019), 17A128 (exp. 03/2021), W00103 (exp. 06/2019), 16A071, 17A130, 16C076, 15D081, W00095, 15K016, W0135, 15D007, 15D080, 16B174, 16A078, 16D065, 16B041, W0176, 15D115, 16A214.
    Where it was sold
    Nationwide throughout the United States and United Kingdom, Mexico, Netherlands, Sweden, Australia, Canada, Hong Kong, Spain, New Zealand, Chile, Taiwan, Switzerland, Albania, Poland, Israel, Monaco, Japan, India, Hungary, Saudi Arabia, Malaysia, UAE, Norway, France, Russia, Australia, Colombia, Czech Republic, Nigeria, Ireland, Philippines
    Amount recalled
    290,000 units
    Status
    Ended Feb 8, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1675-2018
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Jun 29, 2018

    3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4.4 oz, yellow package, UPC: 6 919892 633101

    Product contains undeclared milk.

    May Flower International Inc. · Maspeth, NY

    Where it was sold: New York

    UPC 6919892633101
    Show details
    Product, as FDA describes it
    3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4.4 oz, yellow package, UPC: 6 919892 633101
    Reason, in FDA's words
    Product contains undeclared milk.
    Codes on the package
    No codes.
    Where it was sold
    New York
    Amount recalled
    8 cases
    Status
    Ended Aug 2, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1676-2018
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Jun 28, 2018

    Wish Bone House Italian Salad Dressing 15 oz.

    The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not...

    Pinnacle Food Group, Llc · Cherry Hill, NJ

    Where it was sold: 73 locations received the product. The locations are a mix of retailers and distributors. Product was distributed nationwide to receiving locations in 31 states.

    Show details
    Product, as FDA describes it
    Wish Bone House Italian Salad Dressing 15 oz.
    Reason, in FDA's words
    The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.
    Codes on the package
    Item number 004132100648 Case Lot Code 4913019S51
    Where it was sold
    73 locations received the product. The locations are a mix of retailers and distributors. Product was distributed nationwide to receiving locations in 31 states.
    Amount recalled
    7,768 cases
    Status
    Ended Nov 17, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1655-2018
    View in FDA's recall database
  12. ENDEDClass III · Low riskRecalled Jun 21, 2018

    Blue Bell Ice Cream, Brand Homemade Vanilla Flavored, 3 FL OZ (88 mL), Cups, 24 per box, This Unit N...

    Vanilla ice cream not labeled for individual sale was distributed to stores for individual sale. They are therefore missing a nutrition facts panel, a...

    Blue Bell Creameries, L.P. · Brenham, TX

    Where it was sold: AL, GA, LA, MS, NC, OK, TX

    Show details
    Product, as FDA describes it
    Blue Bell Ice Cream, Brand Homemade Vanilla Flavored, 3 FL OZ (88 mL), Cups, 24 per box, This Unit Not Labeled For Retail Sale
    Reason, in FDA's words
    Vanilla ice cream not labeled for individual sale was distributed to stores for individual sale. They are therefore missing a nutrition facts panel, an ingredients statement , and they do not declare the presence of the major food allergen milk
    Codes on the package
    Code Date: 051020584; Best By Date: 5/10/2020
    Where it was sold
    AL, GA, LA, MS, NC, OK, TX
    Amount recalled
    136 boxes
    Status
    Ended Aug 9, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1614-2018
    View in FDA's recall database
  13. ENDEDClass I · Most seriousRecalled Jun 21, 2018

    Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in quilon parchment paper with a sticker lab...

    Honey Mama's Oregon Peppermint Cacao-Nectar Bar, 2.5 oz, is recalled due to undeclared almonds.

    Nectar Foods LLC · Portland, OR

    Where it was sold: Product is sold on website HoneyMamas.com and distributed in Arkansas, California, Delaware, Florida, Georgia, Louisiana, Massachusetts, New Jersey, New York, North Carolina, Ohio,...

    Show details
    Product, as FDA describes it
    Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in quilon parchment paper with a sticker label. Net wt. 2.5 oz, 3" x 3" bar, 12 bars to a cardboard display case and 12 display cases to a cardboard master case. UPC on each bar is 8 54835 00402 9. The product label is read in parts: "***Paleo HONEY MAMA'S***Oregon Peppermint CACAO-NECTAR BAR ***Made with luscious coconut meat, dark cocoa, peppermint oil & raw local honey*** NO Gluten, Soy, Dairy or Grain *** INGREDIENTS: raw local honey, shredded Organic coconut, unrefined Organic coconut oil, Organic Dutch alkalized cocoa powder, Himalayan pink salt, peppermint oil***Contains tree nut (coconut).
    Reason, in FDA's words
    Honey Mama's Oregon Peppermint Cacao-Nectar Bar, 2.5 oz, is recalled due to undeclared almonds.
    Codes on the package
    121918
    Where it was sold
    Product is sold on website HoneyMamas.com and distributed in Arkansas, California, Delaware, Florida, Georgia, Louisiana, Massachusetts, New Jersey, New York, North Carolina, Ohio, Oregon, Texas, Utah, Virginia, Vermont, Washington and Wisconsin.
    Amount recalled
    79 display cases or sleeves (948 bars total)
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1654-2018
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Jun 20, 2018

    Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068

    Cups containing coconut skyr yogurt may have been mislabeled as vanilla skyr yogurt.

    Icelandic Provisions Inc. · New York, NY

    Where it was sold: NY, NJ, MA, TX, MD, CT, NH, ME, WA

    UPC 854074006068
    Show details
    Product, as FDA describes it
    Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068
    Reason, in FDA's words
    Cups containing coconut skyr yogurt may have been mislabeled as vanilla skyr yogurt.
    Codes on the package
    AUG022018
    Where it was sold
    NY, NJ, MA, TX, MD, CT, NH, ME, WA
    Amount recalled
    1,884 cases (22,608 cups)
    Status
    Ended Oct 4, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1606-2018
    View in FDA's recall database
  15. ENDEDClass III · Low riskRecalled Jun 12, 2018

    Melissa's Spicy Edamame: Lightly seasoned with Japanese Chile and Sesame Oil. 7 oz. (1.98g) Keep ...

    The incorrect spice packet was included in the product package. The spice mix contains oyster sauce which is listed in ingredient or allergen statemen...

    World Variety Produce Inc. · Vernon, CA

    Where it was sold: Arizona, California, Georgia, Indiana, Louisiana, New Mexico, Nevada, Ohio, Pennsylvania, and Texas.

    UPC 045255146370
    Show details
    Product, as FDA describes it
    Melissa's Spicy Edamame: Lightly seasoned with Japanese Chile and Sesame Oil. 7 oz. (1.98g) Keep Refrigerated UPC: 0-45255-14637 6 count and 12 count cases; Ingredients: Soybeans, water Sesame oil, Soy Sauce (soy Beans, Wheat and salt) Rice Wine vinegar, Chaotian chile, pepper, sugar, garlic, sodium glutamate. Flavoring packet included contains oyster sauce that is not declared. Label does state that product is manufactured in a facility that processes milk, egg, shellfish, tree nuts and peanuts. Distributed by World Variety Produce inc. Los Angeles, CA
    Reason, in FDA's words
    The incorrect spice packet was included in the product package. The spice mix contains oyster sauce which is listed in ingredient or allergen statement.
    Codes on the package
    Best Used by Dates of 5/29/1 through 7/2/2018.: 13682403 05/29/18 13754403 06/01/18 13814101 06/05/18 13861501 06/07/18 13883102 06/07/18 13928603 06/12/18 13935404 06/12/18 13957202 06/14/18 14054601 06/20/18 14024302 06/20/18 14110401 06/25/18 14159204 06/26/18 14216503 06/29/18 6 count lot number and expiry date: 13685402 05/30/18 13708303 05/30/18 13685902 06/01/18 13779302 06/01/18 13708402 06/04/18 13783102 06/05/18 13814405 06/06/18 13834402 06/06/18 13832902 06/07/18 13883102 06/07/18 13883203 06/08/18 13861304 06/08/18 13934601 06/11/18 13935404 06/12/18 13950503 06/12/18 13957203 06/14/18 14000403 06/15/18 13985504 06/15/18 14007802 06/15/18 14019602 06/15/18 14024302 06/20/18 14056802 06/21/18 14110403 06/25/18 14159205 06/26/18 14166702 06/26/18 14185102 06/27/18 14185302 06/28/18 14201502 06/29/18 14233501 06/29/18 14236902 07/02/18
    Where it was sold
    Arizona, California, Georgia, Indiana, Louisiana, New Mexico, Nevada, Ohio, Pennsylvania, and Texas.
    Amount recalled
    1662 cases
    Status
    Ended Oct 10, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1583-2018
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Jun 4, 2018

    BLUEBERRY PRETZEL, NET WEIGHT : 4OZ (113g) ,USE BY DATE : 12/1/2018

    Four Link Nutriworld has initiated a recall of NATURAL WHOLE NUT - BLUEBERRY PRETZEL, 4.0z, used by date of 12/01/2018 because of mislabeled product. ...

    Four Link Nutriworld · Clifton, NJ

    Where it was sold: The product was distributed to only NY area. All the accounts are retail grocery stores.

    Show details
    Product, as FDA describes it
    BLUEBERRY PRETZEL, NET WEIGHT : 4OZ (113g) ,USE BY DATE : 12/1/2018
    Reason, in FDA's words
    Four Link Nutriworld has initiated a recall of NATURAL WHOLE NUT - BLUEBERRY PRETZEL, 4.0z, used by date of 12/01/2018 because of mislabeled product. The "MILK" ingredient was omitted in the ingredient section. Blueberry Pretzel has a coating that includes milk content. This can cause milk allergen to people who are allergic to milk.
    Codes on the package
    Not listed
    Where it was sold
    The product was distributed to only NY area. All the accounts are retail grocery stores.
    Amount recalled
    30 CONTAINERS of 4 oz (113g) blueberry pretzels
    Status
    Ended Mar 3, 2022 (FDA lists it as terminated)
    FDA recall number
    F-1610-2018
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled May 30, 2018

    BISCUIT FOOD Cheese Biscuits, The product comes in a 16.5 oz. (468g), clear plastic package. The pro...

    Product contains undeclared milk.

    SDQ Trading Inc. · Brooklyn, NY

    Where it was sold: Retailers in NY

    UPC 6926145714029UPC 6926145712902
    Show details
    Product, as FDA describes it
    BISCUIT FOOD Cheese Biscuits, The product comes in a 16.5 oz. (468g), clear plastic package. The product UPC codes 6926145714029 and 6926145712902. Manufacturer: Dongguan Jiayou Food Co., Ltd. Product of China.
    Reason, in FDA's words
    Product contains undeclared milk.
    Codes on the package
    All lot codes.
    Where it was sold
    Retailers in NY
    Amount recalled
    Cannot be determined
    Status
    Ended Mar 25, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1575-2018
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled May 29, 2018

    Meijer DILL PICKLE FLAVORED CLASSIC CRUNCH POTATO CHIPS***UPC 719283594365***LOT CODE***

    Milk allergen was not declared on the labeling of the product.

    Shearers Foods, Llc · Massillon, OH

    Where it was sold: Products were distributed in Michigan only to their distributor. However, products were eventually distributed to OH, MI, IN, IL, KY and WI.

    UPC 719283594365
    Show details
    Product, as FDA describes it
    Meijer DILL PICKLE FLAVORED CLASSIC CRUNCH POTATO CHIPS***UPC 719283594365***LOT CODE***
    Reason, in FDA's words
    Milk allergen was not declared on the labeling of the product.
    Codes on the package
    UPC: 719283594365 Lot Code 04110831 Sell By 07/16/18 Lot Code 04210831 Sell By 07/16/18 Lot Code 04311632 Sell By 07/16/18 Lot Code 04111732 Sell By 07/16/18 Lot Code 04312430 Sell By 07/23/18 Lot Code 04213135 Sell By 07/30/18 Lot Code 04114434 Sell By 08/13/18
    Where it was sold
    Products were distributed in Michigan only to their distributor. However, products were eventually distributed to OH, MI, IN, IL, KY and WI.
    Amount recalled
    2273 Cases with 11 bags (9.5 oz) per case
    Status
    Ended Feb 14, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1541-2018
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled May 29, 2018

    Milk Chocolate Covered Fudge Bites, 3.75oz, PET Pouch, 12 packages per case

    Morley Candy Makers, Inc. initiated a voluntary recall of Sanders Milk Chocolate Covered Fudge Bites due to undeclared allergen almonds (treenuts).

    Morley Candy Makers, Inc. · Clinton Township, MI

    Where it was sold: Domestic Only: CA, FL, IL, MI, NJ, OH, OK, WI

    UPC 035900296130
    Show details
    Product, as FDA describes it
    Milk Chocolate Covered Fudge Bites, 3.75oz, PET Pouch, 12 packages per case
    Reason, in FDA's words
    Morley Candy Makers, Inc. initiated a voluntary recall of Sanders Milk Chocolate Covered Fudge Bites due to undeclared allergen almonds (treenuts).
    Codes on the package
    UPC Code: 0 35900 29613 0 Lot Code: 8109 FL Best By January 31, 2019
    Where it was sold
    Domestic Only: CA, FL, IL, MI, NJ, OH, OK, WI
    Amount recalled
    330.42 cases (3965 pouches)
    Status
    Ended Feb 7, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1549-2018
    View in FDA's recall database
  20. ENDEDClass III · Low riskRecalled May 25, 2018

    Herd of Turtles confection milk chocolate, 4 oz. and 8 oz. packages. UPC of 4 oz: 6 55974 89004 ...

    Herd of Turtles confection milk chocolate is recalled because pecan is listed on the Ingredients statement but it is not listed in the Contains statem...

    Yukon Jackson · Seattle, WA

    Where it was sold: distributed in WA

    Show details
    Product, as FDA describes it
    Herd of Turtles confection milk chocolate, 4 oz. and 8 oz. packages. UPC of 4 oz: 6 55974 89004 3. UPC of 8 oz: 6 55974 89008 1. The label is read in parts: "***INGREDIENTS: MILK CHOCOLATE 35% (SUGAR, COCOA BUTTER, WHOLE MILK POWDER, EMULSIFIER, SOYA LECITHIN, VANILLA), CARAMEL (SUGAR, CREAM, MILK, CORN SYRUP, COCOA BUTTER), PECANS, NATURAL VANILLA*** CONTAINS: MILK & SOYA***".
    Reason, in FDA's words
    Herd of Turtles confection milk chocolate is recalled because pecan is listed on the Ingredients statement but it is not listed in the Contains statement.
    Codes on the package
    no codes
    Where it was sold
    distributed in WA
    Amount recalled
    11 cs + 2 # bulk of 8 oz and 208 units of 4 oz
    Status
    Ended Jun 25, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1576-2018
    View in FDA's recall database

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What the classes mean

Class I · Most serious. FDA's highest level: products that could cause serious health problems or death.

Class II · Moderate. It may cause temporary health problems, or the risk of serious harm is remote.

Class III · Low risk. Not likely to cause health problems, but it breaks a labeling or manufacturing rule.

If you have a recalled product

  1. Match the codes on your package to the recall.
  2. If they match, don't eat it.
  3. Return it to the store or throw it away, as the company directs.
  4. If you feel sick, contact your doctor.

At the store?

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Recall information comes from FDA's enforcement reports through openFDA. FDA publishes new reports weekly; we check every recall's status daily. This page is for information only and is not medical advice. Meat, poultry and egg products are recalled by USDA, not FDA, and are not listed here.