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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

3,338 ended recalls · showing 1,881 to 1,900

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  1. ENDEDClass II · ModerateRecalled Mar 14, 2018

    Roast Beef Gravy Seasoning Manufacturer's code: PF07040000 packaged in a multi-walled paper bag with...

    Potential for Salmonella contamination.

    Precise Food Ingredients, Inc. · Carrollton, TX

    Where it was sold: Texas

    Show details
    Product, as FDA describes it
    Roast Beef Gravy Seasoning Manufacturer's code: PF07040000 packaged in a multi-walled paper bag with poly liner, 28 pounds
    Reason, in FDA's words
    Potential for Salmonella contamination.
    Codes on the package
    Lot numbers: WO25251 and WO25043
    Where it was sold
    Texas
    Amount recalled
    896 pounds
    Status
    Ended May 7, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1010-2018
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A

    Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.

    Avalon Packaging · Orem, UT

    Where it was sold: Sold to Label owner in UT.

    Show details
    Product, as FDA describes it
    NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A
    Reason, in FDA's words
    Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.
    Codes on the package
    Lot 171409
    Where it was sold
    Sold to Label owner in UT.
    Amount recalled
    1108 bottles
    Status
    Ended Jan 22, 2020 (FDA lists it as terminated)
    FDA recall number
    F-0996-2018
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    RED Vein Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The...

    Kraken Kratom, Phytoextractum, and Soul Speciosa products containing Red Vein Kratom Powder are recalled due to potential contamination with Salmonell...

    Pdx Aromatics · Portland, OR

    Where it was sold: distributed throughout the U.S.

    Show details
    Product, as FDA describes it
    RED Vein Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder is packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), and 112 grams (4 ounces). The varieties under each brand include: -Maeng Da Thai Kratom Powder (Horn Red) -Red Dragon Kratom Powder -Red Vein Borneo Kratom Powder -Red Vein Sumatra Kratom Powder -Red Vein Thai Kratom Powder -Super Indo Kratom Powder
    Reason, in FDA's words
    Kraken Kratom, Phytoextractum, and Soul Speciosa products containing Red Vein Kratom Powder are recalled due to potential contamination with Salmonella.
    Codes on the package
    The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20180118 LOT 20180119 LOT 20180120 LOT 20180121 LOT 20180122 LOT 20180123 LOT 20180124 LOT 20180125 LOT 20180126 LOT 20180127 LOT 20180128 LOT 20180129 LOT 20180130 LOT 20180131 LOT 20180201 LOT 20180201 LOT 20180202 LOT 20180203 LOT 20180204 LOT 20180205 LOT 20180206 LOT 20180207 LOT 20180208 LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 EXPANDED (on 3/16/18) recalled red vein products have the following lot numbers: LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308 ************************************************************************* Second EXPANDED (3/22/18) recalled red vein powder have the following lot numbers: LOT 20171201 LOT 20171202 LOT 20171203 LOT 20171204 LOT 20171205 LOT 20171206 LOT 20171207 LOT 20171208 LOT 20171209 LOT 20171210 LOT 20171211 LOT 20171212 LOT 20171213 LOT 20171214 LOT 20171215 LOT 20171216 LOT 20171217 LOT 20171218 LOT 20171219 LOT 20171220 LOT 20171221 LOT 20171222 LOT 20171223 LOT 20171224 LOT 20171225 LOT 20171226 LOT 20171227 LOT 20171228 LOT 20171229 LOT 20171230 LOT 20171231 LOT 20180101 LOT 20180102 LOT 20180103 LOT 20180104 LOT 20180105 LOT 20180106 LOT 20180107 LOT 20180108 LOT 20180109 LOT 20180110 LOT 20180111 LOT 20180112 LOT 20180113 LOT 20180114 LOT 20180115 LOT 20180116 LOT 20180117 LOT 20180118 LOT 20180119 LOT 20180120 LOT 20180121 LOT 20180122 LOT 20180122 LOT 20180124 LOT 20180125 LOT 20180126 LOT 20180127 LOT 20180128 LOT 20180129 LOT 20180130 LOT 20180131 LOT 20180201 LOT 20180202 LOT 20180203 LOT 20180204 LOT 20180205 LOT 20180206 LOT 20180207 LOT 20180208 LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308
    Where it was sold
    distributed throughout the U.S.
    Amount recalled
    18572 packages
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1523-2018
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    WHITE VEIN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. T...

    Kraken Kratom, Phytoextractum, and Soul Speciosa products containing WHITE VEIN Kratom Powder are recalled due to potential contamination with Salmone...

    Pdx Aromatics · Portland, OR

    Where it was sold: distributed throughout the U.S.

    Show details
    Product, as FDA describes it
    WHITE VEIN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder is packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces), and 225 grams. The varieties under each brand include: Kraken Kratom Maeng Da Thai Kratom Powder (White Vein) Kraken Kratom White Vein Borneo Kratom Powder Kraken Kratom White Vein Sumatra Powder Phytoextractum White Maeng Da Powder (including 225 g) Phytoextractum White Borneo Powder (including 225 g) Phytoextractum White Vein Sumatra Powder Soul Speciosa Borneo Kratom Powder (White Vein) Soul Speciosa Sumatra Kratom Powder (White Vein)
    Reason, in FDA's words
    Kraken Kratom, Phytoextractum, and Soul Speciosa products containing WHITE VEIN Kratom Powder are recalled due to potential contamination with Salmonella.
    Codes on the package
    The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308
    Where it was sold
    distributed throughout the U.S.
    Amount recalled
    4,676 packages total
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1524-2018
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    WHITE VEIN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa....

    Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.

    Pdx Aromatics · Portland, OR

    Where it was sold: distributed throughout the U.S.

    Show details
    Product, as FDA describes it
    WHITE VEIN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom White Vein Borneo Kratom Capsules Phytoextractum White Maeng Da Thai Capsules Soul Speciosa White Vein Borneo Kratom Capsules
    Reason, in FDA's words
    Kraken Kratom, Phytoextractum, and Soul Speciosa WHITE VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
    Codes on the package
    The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308
    Where it was sold
    distributed throughout the U.S.
    Amount recalled
    1097 packages total
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1525-2018
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    GREEN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. ...

    Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.

    Pdx Aromatics · Portland, OR

    Where it was sold: distributed throughout the U.S.

    Show details
    Product, as FDA describes it
    GREEN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom Bali Capsules Phytoextractum OG Bali Capsules Soul Speciosa Bali Capsules
    Reason, in FDA's words
    Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom CAPSULES are recalled due to potential contamination with Salmonella.
    Codes on the package
    The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308
    Where it was sold
    distributed throughout the U.S.
    Amount recalled
    3197 packages
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1526-2018
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    GREEN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. Th...

    Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella.

    Pdx Aromatics · Portland, OR

    Where it was sold: distributed throughout the U.S.

    Show details
    Product, as FDA describes it
    GREEN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom OG Bali Powder Kraken Kratom Super Green Malaysian Kratom Powder Phytoextractum OG Bali Powder Phytoextractum Green Vein Thai Kratom Powder Phytoextractum Super Green Malaysian Kratom Powder Soul Speciosa OG Bali Powder Soul Speciosa Thai Kratom Powder (Green Vein) Soul Speciosa Super Green Malaysian Kratom Powder
    Reason, in FDA's words
    Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER are recalled due to potential contamination with Salmonella.
    Codes on the package
    The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308 Additionally, the GREEN VEIN powder products EXCEPT OG Bali Powder listed below have any of the following LOT codes: LOT 20170918 LOT 20170919 LOT 20170920 LOT 20170921 LOT 20170922 LOT 20170923 LOT 20170924 LOT 20170925 LOT 20170926 LOT 20170927 LOT 20170928 LOT 20170929 LOT 20170930 LOT 20171001 LOT 20171002 LOT 20171003 LOT 20171004 LOT 20171005 LOT 20171006 LOT 20171007 LOT 20171008 LOT 20171009 LOT 20171010 LOT 20171011 LOT 20171012 LOT 20171013 LOT 20171014 LOT 20171015 LOT 20171016 LOT 20171017 LOT 20171018 LOT 20171019 LOT 20171020 LOT 20171021 LOT 20171022 LOT 20171023 LOT 20171024 LOT 20171025 LOT 20171026 LOT 20171027 LOT 20171028 LOT 20171029 LOT 20171030 LOT 20171031 LOT 20171101
    Where it was sold
    distributed throughout the U.S.
    Amount recalled
    20,546 pkgs.
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1527-2018
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Mar 9, 2018

    RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. Th...

    Kraken Kratom, Phytoextractum, and Soul Speciosa RED VEin Kratom Capsule are recalled due to potential contamination with Salmonella.

    Pdx Aromatics · Portland, OR

    Where it was sold: distributed throughout the U.S.

    Show details
    Product, as FDA describes it
    RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include: Kraken Kratom Red Maeng Da Capsules Phytoextractum Red Maeng Da Thai Capsules Soul Speciosa Red Maeng Da Capsules
    Reason, in FDA's words
    Kraken Kratom, Phytoextractum, and Soul Speciosa RED VEin Kratom Capsule are recalled due to potential contamination with Salmonella.
    Codes on the package
    The lot code represents the day packaged. The first four digits are the year, followed by two digits for the month, followed by two digits for the day. LOT 20171201 LOT 20171202 LOT 20171203 LOT 20171204 LOT 20171205 LOT 20171206 LOT 20171207 LOT 20171208 LOT 20171209 LOT 20171210 LOT 20171211 LOT 20171212 LOT 20171213 LOT 20171214 LOT 20171215 LOT 20171216 LOT 20171217 LOT 20171218 LOT 20171219 LOT 20171220 LOT 20171221 LOT 20171222 LOT 20171223 LOT 20171224 LOT 20171225 LOT 20171226 LOT 20171227 LOT 20171228 LOT 20171229 LOT 20171230 LOT 20171231 LOT 20180101 LOT 20180102 LOT 20180103 LOT 20180104 LOT 20180105 LOT 20180106 LOT 20180107 LOT 20180108 LOT 20180109 LOT 20180110 LOT 20180111 LOT 20180112 LOT 20180113 LOT 20180114 LOT 20180115 LOT 20180116 LOT 20180117 LOT 20180118 LOT 20180119 LOT 20180120 LOT 20180121 LOT 20180122 LOT 20180122 LOT 20180124 LOT 20180125 LOT 20180126 LOT 20180127 LOT 20180128 LOT 20180129 LOT 20180130 LOT 20180131 LOT 20180201 LOT 20180202 LOT 20180203 LOT 20180204 LOT 20180205 LOT 20180206 LOT 20180207 LOT 20180208 LOT 20180209 LOT 20180210 LOT 20180211 LOT 20180212 LOT 20180213 LOT 20180214 LOT 20180215 LOT 20180216 LOT 20180217 LOT 20180218 LOT 20180219 LOT 20180220 LOT 20180221 LOT 20180222 LOT 20180223 LOT 20180224 LOT 20180225 LOT 20180226 LOT 20180227 LOT 20180228 LOT 20180301 LOT 20180302 LOT 20180303 LOT 20180304 LOT 20180305 LOT 20180306 LOT 20180307 LOT 20180308
    Where it was sold
    distributed throughout the U.S.
    Amount recalled
    10,210 packages
    Status
    Ended Sep 13, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1528-2018
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Mar 6, 2018

    Cardamom Pods Green Whole Organic Sold in 25 lb. bulk boxes and 1 lb. retail plastic bags UPC...

    Customer notified firm after they received a positive result for Salmonella of Lot #90186-00 Cardamon Pods Green Whole Organic supplied by Starwest Bo...

    Starwest Botanicals, Inc · Sacramento, CA

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

    Where it was sold: US and Canada

    Show details
    Product, as FDA describes it
    Cardamom Pods Green Whole Organic Sold in 25 lb. bulk boxes and 1 lb. retail plastic bags UPC 1 pound bags: 7-6796302528-9; UPC bulk: 7 679630257-2 Imported from Guatemala Starwest Botanicals, Sacramento, CA
    Reason, in FDA's words
    Customer notified firm after they received a positive result for Salmonella of Lot #90186-00 Cardamon Pods Green Whole Organic supplied by Starwest Botanicals
    Codes on the package
    Bulk lot #90186-00, Item number 1 lb. bags lot 75593, Item number 209735-01
    Where it was sold
    US and Canada
    Amount recalled
    810 pounds of bulk and 133 x 1 lb. bags
    Status
    Ended Jul 6, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0971-2018
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Jan 22, 2018

    Prickly Ash Bark Powder Herbal Supplement, packaged in food grade stand up plastic pouches or plasti...

    Prickly Ash Bark Powder is recalled due to a potential contamination with Salmonella.

    Mountain Rose Inc · Eugene, OR

    Where it was sold: distributed in AK, AR, AZ, CA, CO , FL, GA, IA, IL, IN, KY, MI, NC, NE, NH, NJ, NS, NV, NY, OH, OR, PA, SC, TX, UT, VA, VT, WA, WI, and WY.

    Show details
    Product, as FDA describes it
    Prickly Ash Bark Powder Herbal Supplement, packaged in food grade stand up plastic pouches or plastic bags depending on quantity ordered, various net weights - 1-oz., 4-oz., 8-oz., 1-lb., 2-lb., 5-lb., 7-lb., 11-lb., 15-lb., and 16-lb. The label is read in parts: "***Prickly Ash Bark Powder***Zanthoxylum clava-herculis***Herbal Supplement***MOUNTAIN ROSE HERBS***EUGENE, OR 97402***".
    Reason, in FDA's words
    Prickly Ash Bark Powder is recalled due to a potential contamination with Salmonella.
    Codes on the package
    Lot #23574-P
    Where it was sold
    distributed in AK, AR, AZ, CA, CO , FL, GA, IA, IL, IN, KY, MI, NC, NE, NH, NJ, NS, NV, NY, OH, OR, PA, SC, TX, UT, VA, VT, WA, WI, and WY.
    Amount recalled
    (25) 1 oz,; (20) 4 oz,; (14) 8 oz,; (23) 1 lb.; (3) 2 lb.; (1) 5 lb.; (1) 7 lb.; (1) 11 lb.; (1) 15 lb.; (1) 16 lb.
    Status
    Ended May 1, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0757-2018
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Jan 20, 2018

    Arthri-D 120ct

    Product may be contaminated with Salmonella.

    ABH Nature's Products, Inc. · Edgewood, NY

    Where it was sold: Direct to MA and PA

    Show details
    Product, as FDA describes it
    Arthri-D 120ct
    Reason, in FDA's words
    Product may be contaminated with Salmonella.
    Codes on the package
    Lot# 1701-092
    Where it was sold
    Direct to MA and PA
    Amount recalled
    10,100 bottles
    Status
    Ended Jun 19, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0812-2018
    View in FDA's recall database
  12. ENDEDClass I · Most seriousRecalled Jan 20, 2018

    Zero for Him 150 count

    Product may be contaminated with Salmonella.

    ABH Nature's Products, Inc. · Edgewood, NY

    Where it was sold: Direct to MA and PA

    Show details
    Product, as FDA describes it
    Zero for Him 150 count
    Reason, in FDA's words
    Product may be contaminated with Salmonella.
    Codes on the package
    Lot#1710638B
    Where it was sold
    Direct to MA and PA
    Amount recalled
    1,137 bottles
    Status
    Ended Jun 19, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0813-2018
    View in FDA's recall database
  13. ENDEDClass I · Most seriousRecalled Jan 16, 2018

    Cherry Tomatoes, packaged in a pint sized plastic clamshell, no labeling

    Frog Holler Produce initiated a voluntary recall of cherry tomatoes, packaged in a pint sized plastic clamshell due to potential contamination with Sa...

    Frog Holler Ltd. · Ann Arbor, MI

    Where it was sold: Domestic: MI Foreign/VA/DOD: None

    Show details
    Product, as FDA describes it
    Cherry Tomatoes, packaged in a pint sized plastic clamshell, no labeling
    Reason, in FDA's words
    Frog Holler Produce initiated a voluntary recall of cherry tomatoes, packaged in a pint sized plastic clamshell due to potential contamination with Salmonella.
    Codes on the package
    No lot codes, best by dates, or identifying labeling; product was distributed between 01/04/2018 and 01/10/2018.
    Where it was sold
    Domestic: MI Foreign/VA/DOD: None
    Amount recalled
    16 cases
    Status
    Ended Apr 6, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0702-2018
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Jan 2, 2018

    Coconut Tree Brand Shredded Coconut; frozen Dua Bao; Net WT. 16 oz. (454 g); Product of Vietnam; ...

    State of Massachusetts tested product and found it to be positive for Salmonella

    Evershing International Trading Inc. · San Jose, CA

    Where it was sold: CA, IL, CO, TX, WA, MA, FL, PA, WA, OR, OH,

    UPC 005216440817
    Show details
    Product, as FDA describes it
    Coconut Tree Brand Shredded Coconut; frozen Dua Bao; Net WT. 16 oz. (454 g); Product of Vietnam; UPC 05216-44081 Ingredient: Coconut Manufactured by: Lucky Shing Co., LTD 108/1 Road No. 830, Hamlet No. 3 An Thanh Village, Ben Luc District Long An Province, Vietnam.
    Reason, in FDA's words
    State of Massachusetts tested product and found it to be positive for Salmonella
    Codes on the package
    All lots, item number 331233 Affected lot number is SE07A1; however that number is only on the outer case and not on individual bags.
    Where it was sold
    CA, IL, CO, TX, WA, MA, FL, PA, WA, OR, OH,
    Amount recalled
    4377 cases (40 x 16 oz. bags per case)
    Status
    Ended Feb 28, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0567-2018
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Nov 2, 2017

    GOYA Adobo, All Purpose Seasoning with Pepper, Goya Foods, Inc. 28 OZ

    Positive results for Salmonella from environmental test conducted at plant and finished product.

    Tradewind Foods de Puerto Rico Inc. · Bayamon, PR

    Where it was sold: P.R. consignees only.

    Show details
    Product, as FDA describes it
    GOYA Adobo, All Purpose Seasoning with Pepper, Goya Foods, Inc. 28 OZ
    Reason, in FDA's words
    Positive results for Salmonella from environmental test conducted at plant and finished product.
    Codes on the package
    Best By: 10/23/22
    Where it was sold
    P.R. consignees only.
    Amount recalled
    6864 units (572 cases)
    Status
    Ended Jun 27, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0506-2018
    View in FDA's recall database
  16. ENDEDClass I · Most seriousRecalled Nov 2, 2017

    GOYA Adobo, All Purpose Seasoning with Cumin, Goya Foods, Inc. 28 OZ

    Positive results for Salmonella from environmental test conducted at plant and finished product.

    Tradewind Foods de Puerto Rico Inc. · Bayamon, PR

    Where it was sold: P.R. consignees only.

    Show details
    Product, as FDA describes it
    GOYA Adobo, All Purpose Seasoning with Cumin, Goya Foods, Inc. 28 OZ
    Reason, in FDA's words
    Positive results for Salmonella from environmental test conducted at plant and finished product.
    Codes on the package
    Best By: 10/18/22
    Where it was sold
    P.R. consignees only.
    Amount recalled
    1236 units (103 cases)
    Status
    Ended Jun 27, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0507-2018
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Oct 16, 2017

    Newport -Yellowfin Tuna Loin; (3/5 lbs. and 5/8 lbs.) Frozen, packed in 30 lb. (480 oz.) 13.61 KG c...

    Salmonella found in FDA samples of tuna loins.

    RELISH FOODS, INC. · Culver City, CA

    Where it was sold: U.S. distribution to the following: OR, WA, CA, AZ, ID, MT, NV, UT, WY, CO. No foreign distribution.

    Show details
    Product, as FDA describes it
    Newport -Yellowfin Tuna Loin; (3/5 lbs. and 5/8 lbs.) Frozen, packed in 30 lb. (480 oz.) 13.61 KG cardboard box. Product of Indonesia. Ingredients: Yellowfin tuna (fish), Water, carbon monoxide (for color retention).
    Reason, in FDA's words
    Salmonella found in FDA samples of tuna loins.
    Codes on the package
    Lot Nos. MTNT 0947C, MTNT 0957B, MTNT 0967A, MTNT 0977D MTNT 0917B, MTNT 0937D, GND 0737D, GND 0747E, GND 0757A, GND 0767C, GND 0777B
    Where it was sold
    U.S. distribution to the following: OR, WA, CA, AZ, ID, MT, NV, UT, WY, CO. No foreign distribution.
    Amount recalled
    1,966 Cases
    Status
    Ended Nov 6, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0110-2018
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled Oct 16, 2017

    Newport -Yellowfin Tuna Steaks; (4 oz. and 6 oz.) Frozen, packed in 10 lb. (160 oz.) 4.54 KG cardbo...

    Salmonella found in FDA samples of tuna loins.

    RELISH FOODS, INC. · Culver City, CA

    Where it was sold: U.S. distribution to the following: OR, WA, CA, AZ, ID, MT, NV, UT, WY, CO. No foreign distribution.

    Show details
    Product, as FDA describes it
    Newport -Yellowfin Tuna Steaks; (4 oz. and 6 oz.) Frozen, packed in 10 lb. (160 oz.) 4.54 KG cardboard box. Product of Indonesia. Ingredients: Yellowfin tuna (fish), Water, carbon monoxide (for color retention).
    Reason, in FDA's words
    Salmonella found in FDA samples of tuna loins.
    Codes on the package
    Lot Nos. GND 0697B, GND 0707C, GND 0727A
    Where it was sold
    U.S. distribution to the following: OR, WA, CA, AZ, ID, MT, NV, UT, WY, CO. No foreign distribution.
    Amount recalled
    1,500 Cases
    Status
    Ended Nov 6, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0111-2018
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Oct 9, 2017

    Spicely Organics Organic Tarragon 0.4oz. (11g) UPC codes: 8 26998 04106 7

    Potential Salmonella contamination.

    Organic Spices, Inc · Fremont, CA

    Where it was sold: U.S. distribution to the following: Alaska, Arizona, California, Colorado, Hawaii, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Nevada, New Mexico, New York, Ohio, Ore...

    UPC 826998041067
    Show details
    Product, as FDA describes it
    Spicely Organics Organic Tarragon 0.4oz. (11g) UPC codes: 8 26998 04106 7
    Reason, in FDA's words
    Potential Salmonella contamination.
    Codes on the package
    Lot Number: OTW100134 Best if used by: 12/31/2020
    Where it was sold
    U.S. distribution to the following: Alaska, Arizona, California, Colorado, Hawaii, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Nevada, New Mexico, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington and Wisconsin No foreign distribution.
    Amount recalled
    1570 jars
    Status
    Ended Jan 8, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0131-2018
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Sep 8, 2017

    Maradol Papaya; Frutas Selectas De Tijuana, S. DE R.L. DE, C.V. Sold in 14.00 kg/ 31 Lb. cardbo...

    Firm is recalling Maradol Papaya from Productores y Exportadores de Carica Papaya de Tecom¿n y Costa Alegre SPR of RL and packed by Frutas Selectas de...

    Bravo Produce Inc · San Ysidro, CA

    Where it was sold: Initial distribution in CA only.

    Show details
    Product, as FDA describes it
    Maradol Papaya; Frutas Selectas De Tijuana, S. DE R.L. DE, C.V. Sold in 14.00 kg/ 31 Lb. cardboard boxes.
    Reason, in FDA's words
    Firm is recalling Maradol Papaya from Productores y Exportadores de Carica Papaya de Tecom¿n y Costa Alegre SPR of RL and packed by Frutas Selectas de Tijuana, S. de RL de CV due to Salmonella contamination
    Codes on the package
    Code numbers : 1222335215 1222635220 1222335216 1223035223 1223335227 1223835233 1222235215 1222535220 1222235216 1222835223 1223435230 1222235216 1222935223 1222135214 1222935223 1222935223 1222135214 1222235216 1222935223 1223035223 1222935221 1223035223 1223835233.
    Where it was sold
    Initial distribution in CA only.
    Amount recalled
    8,325 boxes
    Status
    Ended Nov 21, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3560-2017
    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.

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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.