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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

3,539 recalls · showing 2,001 to 2,020

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  1. ENDEDClass I · Most seriousRecalled May 2, 2018

    Acadica Kratom: Green Hulu 2 Kratom, 250g bags

    Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.

    Badger Botanicals LLC · Springville, UT

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    Acadica Kratom: Green Hulu 2 Kratom, 250g bags
    Reason, in FDA's words
    Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due to potential salmonella.
    Codes on the package
    Everything manufactured between 1/1/18 to 4/12/18.
    Where it was sold
    Nationwide
    Amount recalled
    N/A
    Status
    Ended Apr 19, 2022 (FDA lists it as terminated)
    FDA recall number
    F-1465-2018
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Apr 20, 2018

    Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K. Bali Supreme, K Maeng Da Supreme, ...

    FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.

    Eden's Ethnos, LLC · Carlsbad, CA

    Where it was sold: FL, MO, OR, CA, UT

    Show details
    Product, as FDA describes it
    Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K. Bali Supreme, K Maeng Da Supreme, K Green Vein, Green Maeng Da, K Red Maeng Da, K Red Bali, K Green Bali Distributed by Eden Ethnos LLC, Carlsbad, CA 92010
    Reason, in FDA's words
    FDA and state samples found Salmonella in Kratom products that traced back to Eden Ethnos LLC.
    Codes on the package
    No Codes
    Where it was sold
    FL, MO, OR, CA, UT
    Amount recalled
    2,775 kilograms
    Status
    Ended Jun 25, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1439-2018
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Apr 18, 2018

    Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, so...

    Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali Kratom products are being recalled because they have...

    Viable Solutions, LLC · Nampa, ID

    Where it was sold: Nationwide through internet sales

    Show details
    Product, as FDA describes it
    Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Red Vein Sumatra***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.COM***". The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Red Vein Bali***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.COM***".
    Reason, in FDA's words
    Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali Kratom products are being recalled because they have the potential to be contaminated with Salmonella
    Codes on the package
    Recalled product has any of the following LOT Numbers: RVS1380182301; RVB1380182201; GVH1380171512; MD13120181601.
    Where it was sold
    Nationwide through internet sales
    Amount recalled
    350 packages of Red Vein Sumatra and 350 packages of Red Vein Bali
    Status
    Ended Nov 16, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1476-2018
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Apr 18, 2018

    Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powd...

    Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella

    Viable Solutions, LLC · Nampa, ID

    Where it was sold: Nationwide through internet sales

    Show details
    Product, as FDA describes it
    Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Green Horn***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.COM***".
    Reason, in FDA's words
    Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella
    Codes on the package
    Recalled product has any of the following LOT Numbers: RVS1380182301; RVB1380182201; GVH1380171512; MD13120181601.
    Where it was sold
    Nationwide through internet sales
    Amount recalled
    350 packages
    Status
    Ended Nov 16, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1477-2018
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Apr 18, 2018

    Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The p...

    Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella

    Viable Solutions, LLC · Nampa, ID

    Where it was sold: Nationwide through internet sales

    Show details
    Product, as FDA describes it
    Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Thai Maeng Da***Origin: Thailand***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.COM***".
    Reason, in FDA's words
    Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella
    Codes on the package
    Recalled product has any of the following LOT Numbers: RVS1380182301; RVB1380182201; GVH1380171512; MD13120181601.
    Where it was sold
    Nationwide through internet sales
    Amount recalled
    510 packages
    Status
    Ended Nov 16, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1478-2018
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Apr 16, 2018

    Traditional Medicinals Throat Coat Lemon Echinacea; Lemon Echinacea, Naturally Caffeine Free Herbal...

    Vendor has determined that portions of a large raw material lot were positive for Salmonella.

    Traditional Medicinals Inc · Sebastopol, CA

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

    Where it was sold: US distribution and on distributor in Mexico

    UPC 032917001597
    Show details
    Product, as FDA describes it
    Traditional Medicinals Throat Coat Lemon Echinacea; Lemon Echinacea, Naturally Caffeine Free Herbal Tea' 16 wrapped tea bags - Herbal Supplement NET WT 1.13 oz. (32 g) UPC: 32917-00159
    Reason, in FDA's words
    Vendor has determined that portions of a large raw material lot were positive for Salmonella.
    Codes on the package
    Lot Number: 19482; Expiration Date: January 2021
    Where it was sold
    US distribution and on distributor in Mexico
    Amount recalled
    6980 cases (6 cartons per case, 16 teabags per carton)
    Status
    Ended Jun 1, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1142-2018
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Apr 16, 2018

    Traditional Medinicals organic EveryDay Detox Lemon; Naturally Caffeine Free Herbal Tea; 16 wrapp...

    Vendor has determined that portions of a large raw material lot were positive for Salmonella.

    Traditional Medicinals Inc · Sebastopol, CA

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

    Where it was sold: US distribution and on distributor in Mexico

    UPC 032917001979
    Show details
    Product, as FDA describes it
    Traditional Medinicals organic EveryDay Detox Lemon; Naturally Caffeine Free Herbal Tea; 16 wrapped tea bags - Herbal Supplement NET WT .85 oz (24g) UPC: 32917-00197
    Reason, in FDA's words
    Vendor has determined that portions of a large raw material lot were positive for Salmonella.
    Codes on the package
    Lot Number:19461 ; Expiration Date: January 2021
    Where it was sold
    US distribution and on distributor in Mexico
    Amount recalled
    9108 cases (6 cartons per case, 16 teabags per carton)
    Status
    Ended Jun 1, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1143-2018
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Apr 14, 2018

    Shelled Eggs, Extra Large 18pk sold under the brand names of Publix UPC 0 41415 00966 0 & Sunups UPC...

    The firm was notified by their supplier that the product may contain Salmonella.

    Cal Maine Foods · Jackson, MS

    Where it was sold: Product was shipped to FL & GA.

    UPC 041415009660UPC 028621363984
    Show details
    Product, as FDA describes it
    Shelled Eggs, Extra Large 18pk sold under the brand names of Publix UPC 0 41415 00966 0 & Sunups UPC 0 28621 36398 4
    Reason, in FDA's words
    The firm was notified by their supplier that the product may contain Salmonella.
    Codes on the package
    P1539D 048A Best By APR 02 & P1539D 049A Best By APR 03
    Where it was sold
    Product was shipped to FL & GA.
    Amount recalled
    23,400 dz eggs
    Status
    Ended Jul 2, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1411-2018
    View in FDA's recall database
  9. ACTIVEClass I · Most seriousRecalled Apr 13, 2018

    Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

    Shell eggs have the potential to be contaminated with Salmonella Braenderup.

    ROSE ACRE FARM · Seymour, IN

    Where it was sold: Direct consignees located in MS, NJ, GA, VA, FL, NH, NY, AL, NC, CT, MD, UT, & SC retail stores and restaurants via direct delivery.

    Show details
    Product, as FDA describes it
    Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)
    Reason, in FDA's words
    Shell eggs have the potential to be contaminated with Salmonella Braenderup.
    Codes on the package
    Plant Number P-1065; LOT CODES with a Julian date ranged from 011 - 102; Numerous UPCs
    Where it was sold
    Direct consignees located in MS, NJ, GA, VA, FL, NH, NY, AL, NC, CT, MD, UT, & SC retail stores and restaurants via direct delivery.
    Amount recalled
    206,749,248
    Status
    Active (FDA lists it as ongoing)
    FDA recall number
    F-1410-2018
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. T...

    Amaranth Flour is recalled due to potential for contamination with Salmonella.

    Bob's Red Mill Natural Foods, Inc. · Milwaukie, OR

    Where it was sold: Distributed in CA, FL, MI, ND, NH, NY, OH, OR, TX, and WA and in Mexico and United Arab Emirates.

    UPC 039978009111
    Show details
    Product, as FDA describes it
    Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. The label is read in parts: "***Bob's Red Mill ***ORGANIC WHOLE GRAIN AMARANTH FLOUR STONE GROUND*** NET WT 22 OZ ***keeps best refrigerated or frozen***".
    Reason, in FDA's words
    Amaranth Flour is recalled due to potential for contamination with Salmonella.
    Codes on the package
    Sell By 11/26/2015 169617
    Where it was sold
    Distributed in CA, FL, MI, ND, NH, NY, OH, OR, TX, and WA and in Mexico and United Arab Emirates.
    Amount recalled
    2099 cases
    Status
    Ended Jun 8, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1011-2018
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Apr 6, 2018

    HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g

    Product tested positive for salmonella.

    The J.M. Smucker Company, Inc. · Orrville, OH

    Where it was sold: Product was distributed in the following states: AL, CA, FL, HI, IA, IL, IN, KS, LA, MD, MI, MN, MO, MS, NC, ND, NE, NY, OH, OK, PA, TN, TX, VA & WI

    Show details
    Product, as FDA describes it
    HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
    Reason, in FDA's words
    Product tested positive for salmonella.
    Codes on the package
    7331 501, 7332 501, 7333 501
    Where it was sold
    Product was distributed in the following states: AL, CA, FL, HI, IA, IL, IN, KS, LA, MD, MI, MN, MO, MS, NC, ND, NE, NY, OH, OK, PA, TN, TX, VA & WI
    Amount recalled
    9619 cases/12 boxes per case
    Status
    Ended Jul 17, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1107-2018
    View in FDA's recall database
  12. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; ...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1413-2018
    View in FDA's recall database
  13. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Raw Form Organics Maeng Da Kratom Ivory White; 150 capsule and 300 capsule plastic bottles; Manu...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Raw Form Organics Maeng Da Kratom Ivory White; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1414-2018
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Raw Form Organics Maeng Da Kratom Ruby Red; R150 capsule and 300 capsule plastic bottles; Manufa...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Raw Form Organics Maeng Da Kratom Ruby Red; R150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1415-2018
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Raw Form Organics Maeng Da Kratom Amethyst Gold in 150 capsule and 300 capsule plastic bottles; M...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Raw Form Organics Maeng Da Kratom Amethyst Gold in 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1416-2018
    View in FDA's recall database
  16. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Molecule Kratom Red Maeng Da in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Ma...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Molecule Kratom Red Maeng Da in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1417-2018
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Molecule Kratom Green Maeng Da in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; ...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Molecule Kratom Green Maeng Da in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1418-2018
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Molecule Kratom Super Green Malay in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; ...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Molecule Kratom Super Green Malay in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1419-2018
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Molecule Kratom Gold Bali in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manuf...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Molecule Kratom Gold Bali in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1420-2018
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Apr 6, 2018

    Molecule Kratom Red Malay in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manuf...

    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella

    TRIANGLE PHARMANATURALS LLC · Las Vegas, NV

    Where it was sold: WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.

    Show details
    Product, as FDA describes it
    Molecule Kratom Red Malay in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
    Reason, in FDA's words
    All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
    Codes on the package
    ALL
    Where it was sold
    WA, GA, SC, FL, NJ, LA, CA, TX, NV, NC, PA, MO, CO, OR, MT, MA, UT, NE, AZ, MO, NY, OH, VA, MD.
    Amount recalled
    N/A
    Status
    Ended Mar 26, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1421-2018
    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.

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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.