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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 ยท Source: U.S. Food and Drug Administration

28,406 ended recalls ยท showing 1,621 to 1,640

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  1. ENDEDClass II ยท ModerateRecalled Mar 18, 2025

    Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz...

    Potential contamination with patulin.

    S Martinelli & Company ยท Watsonville, CA

    Where it was sold: AL, AR, AZ, CA, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NH, NJ, NY, OH, PA, SC, TX, UT, VA, WI

    Show details
    Product, as FDA describes it
    Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)
    Reason, in FDA's words
    Potential contamination with patulin.
    Codes on the package
    UPC: 0 41244 64102 2 BEST BY: 05DEC2026 Pallet/Batch Numbers: 0001254859, 0001255023, 0001255026, 0001254864, 0001254917, 0001254874, 0001254984, 0001254860, 0001255030, 0001255033, 0001254901, 0001254913, 0001254884, 0001254903, 0001254857, 0001255027, 0001254861, 0001254924, 0001254957, 0001254876, 0001255001, 0001254856, 0001255020, 0001254863, 0001254909, 0001254914, 0001254873, 0001254878, 0001255009, 0001254996, 0001254987, 0001254902, 0001254972, 0001254922, 0001254872, 0001255011, 0001254993, 0001254998, 0001254921, 0001254910, 0001255015, 0001254870, 0001255028, 0001254897, 0001254983, 0001254892, 0001254919, 0001254925, 0001254887, 0001255014, 0001255016, 0001254992, 0001254920, 0001254922, 0001255005, 0001254899, 0001254923, 0001254867, 0001254982, 0001255006, 0001254978, 0001254951, 0001254877, 0001254907, 0001255019, 0001254990, 0001254888, 0001254918, 0001254954, 0001254926, 0001254885, 0001254869, 0001254991, 0001254890, 0001255012, 0001254927, 0001254868, 0001254883, 0001255008, 0001254994, 0001254905, 0001255018, 0001255004, 0001254939, 0001254881, 0001254858, 0001254989, 0001255005, 0001254882, 0001254929, 0001254953, 0001255017, 0001254986, 0001254995, 0001255024, 0001255010, 0001255002, 0001254862, 0001255013, 0001254979, 0001254980, 0001255029, 0001254875, 0001254906, 0001254915, 0001255032, 0001255003, 0001254981, 0001255029, 0001254874, 0001255000, 0001254944, 0001255021, 0001255022, 0001254866, 0001254977, 0001254871, 0001254999, 0001254865, 0001255031, 0001255025, 0001254997, 0001254916, 0001254922, 0001254985
    Where it was sold
    AL, AR, AZ, CA, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NH, NJ, NY, OH, PA, SC, TX, UT, VA, WI
    Amount recalled
    7234 cases
    Status
    Ended Jul 14, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0734-2025
  2. ENDEDClass II ยท ModerateRecalled Mar 17, 2025

    Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, pa...

    Potential foreign material (wood-like material)

    Nestle-USA, Inc. (Corporate Office) ยท Arlington, VA

    Where it was sold: Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, ...

    UPC 013800333131UPC 138005417100
    Show details
    Product, as FDA describes it
    Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per case
    Reason, in FDA's words
    Potential foreign material (wood-like material)
    Codes on the package
    Batch Number: 4214595511, Best By: SEP2025; Product Number: 12531245; Unit UPC: 013800333131; Case UPC: 00138005417100
    Where it was sold
    Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI
    Amount recalled
    7212 cases
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    F-0681-2025
  3. ENDEDClass II ยท ModerateRecalled Mar 17, 2025

    Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, pac...

    Potential foreign material (wood-like material)

    Nestle-USA, Inc. (Corporate Office) ยท Arlington, VA

    Where it was sold: Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, ...

    UPC 013800144065
    Show details
    Product, as FDA describes it
    Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
    Reason, in FDA's words
    Potential foreign material (wood-like material)
    Codes on the package
    Batch: 4261595912, Best By: OCT2025; Batch: 4283595912, Best By: NOV2025; Batch: 4356595912, Best By: JAN2026; Batch: 5018595912, Best By: FEB2026; Batch: 5038595912, Best By: MAR2026; Product Number: 12049225; Unit UPC: 013800144065; Case UPC: 00138001438220
    Where it was sold
    Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI
    Amount recalled
    50611 cases
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    F-0682-2025
  4. ENDEDClass II ยท ModerateRecalled Mar 17, 2025

    Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packag...

    Potential foreign material (wood-like material)

    Nestle-USA, Inc. (Corporate Office) ยท Arlington, VA

    Where it was sold: Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, ...

    UPC 013800558060
    Show details
    Product, as FDA describes it
    Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
    Reason, in FDA's words
    Potential foreign material (wood-like material)
    Codes on the package
    Batch: 4311595912, Best By: DEC2025; Batch: 5002595912, Best By: FEB2026; Batch: 5037595912, Best By: MAR2026; Batch: 5064595912, Best By: APR2026; Product Number: 12340870; Unit UPC: 013800558060; Case UPC: 00138005580770
    Where it was sold
    Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI
    Amount recalled
    25485 cases
    Status
    Ended (FDA lists it as completed)
    FDA recall number
    F-0683-2025
  5. ENDEDClass II ยท ModerateRecalled Mar 17, 2025

    Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benz...

    Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.

    Red Shell Foods, Inc. ยท City Of Industry, CA

    Where it was sold: Primary direct account distribution is within California. Firm is currently working on distribution list information.

    UPC 018529100019
    Show details
    Product, as FDA describes it
    Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benzoate), water, sugar, cooking wine( water, rice, malt), sweet cooking wine(corn syrup, rice, water, malt), modified food starch, dried onion, dried ginger root, dried garlic, lactic acid, spices. "Shake well before use. Keep Refrigerated after opening" UPC# 0-18529-10001-9 (12 ounce) UPC# 0-18529-10505-6 (1 gallon)
    Reason, in FDA's words
    Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.
    Codes on the package
    Lot: 120326 This is also the best by date printed on the container.
    Where it was sold
    Primary direct account distribution is within California. Firm is currently working on distribution list information.
    Amount recalled
    48 bottles (1 gallon size), 933 bottles (12 ounce size)
    Status
    Ended Sep 19, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0696-2025
  6. ENDEDClass I ยท Most seriousRecalled Mar 14, 2025

    Jinga Glass Noodles with vegetables 8 oz. and 12 oz.

    Contains undeclared egg

    HAR Maspeth Corp. ยท Maspeth, NY

    Where it was sold: NY, NJ, MA, CT, PA, MD, NC, IL, MI, GA

    UPC 265405006495UPC 267405004495UPC 266405008496UPC 268405005499
    Show details
    Product, as FDA describes it
    Jinga Glass Noodles with vegetables 8 oz. and 12 oz.
    Reason, in FDA's words
    Contains undeclared egg
    Codes on the package
    Expiration date(s) or Use by Date(s) or expected shelf life of product: 3/13/2025, 3/1/2025, 3/15/2025, 3/16/2025, 3/17/2025, 3/18/2025. UPC Codes: 265405006495, 267405004495, 266405008496, 268405005499 Catalog numbers: 5405, 7405, 6405M, 8405M
    Where it was sold
    NY, NJ, MA, CT, PA, MD, NC, IL, MI, GA
    Amount recalled
    2,627 packages
    Status
    Ended Mar 5, 2026 (FDA lists it as terminated)
    FDA recall number
    F-0663-2025
  7. ENDEDClass II ยท ModerateRecalled Mar 13, 2025

    COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFE...

    Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.

    Massimo Zanetti Beverage USA ยท Suffolk, VA

    Where it was sold: Product was shipped to distribution centers and retail stores in the following states: CO, IA, IL, IN, KS, KY, MI, MN, NC, ND, NE, OH, SD, WI and WY

    UPC 070253110801
    Show details
    Product, as FDA describes it
    COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g) UPC 0 70253 11080 1 DISTRIBUTED BY THE SPARTANNASH COMPANY GRAND RAPIDS, MI 49518
    Reason, in FDA's words
    Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
    Codes on the package
    BEST BEFORE 080325 V 15:37 C
    Where it was sold
    Product was shipped to distribution centers and retail stores in the following states: CO, IA, IL, IN, KS, KY, MI, MN, NC, ND, NE, OH, SD, WI and WY
    Amount recalled
    692cs/6/12oz bags
    Status
    Ended Jul 1, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0666-2025
  8. ENDEDClass II ยท ModerateRecalled Mar 13, 2025

    SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507...

    Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.

    Seabear Company ยท Anacortes, WA

    Where it was sold: Distributed nationwide

    UPC 034507070013
    Show details
    Product, as FDA describes it
    SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.
    Reason, in FDA's words
    Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
    Codes on the package
    64242902SALCH Enjoy by: 10/2028 64242912SALCH Enjoy by: 10/2028 64242972SALCH Enjoy by: 10/2028 64242982SALCH Enjoy by: 10/2028 64243042SALCH Enjoy by: 10/2028 64243052SALCH Enjoy by: 10/2028 64243121SALCH Enjoy by: 11/2028 64243131SALCH Enjoy by: 11/2028 64243191SALCH Enjoy by: 11/2028 64243201SALCH Enjoy by: 11/2028 64243651SALCH Enjoy by: 12/2028 64250031SALCH Enjoy by: 1/2029 64250291SALCH Enjoy by: 1/2029 64250301SALCH Enjoy by: 1/2029
    Where it was sold
    Distributed nationwide
    Amount recalled
    Salmon Chowder = 11,152 pouches
    Status
    Ended Jun 11, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0684-2025
  9. ENDEDClass II ยท ModerateRecalled Mar 13, 2025

    SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 0...

    Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.

    Seabear Company ยท Anacortes, WA

    Where it was sold: Distributed nationwide

    UPC 034507070211
    Show details
    Product, as FDA describes it
    SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
    Reason, in FDA's words
    Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
    Codes on the package
    64241643ALECH Enjoy by: 6/2028 64241641ALECH Enjoy by: 6/2028 64241661ALECH Enjoy by: 6/2028 64243251ALECH Enjoy by: 11/2028 64243261ALECH Enjoy by: 11/2028 64250222ALECH Enjoy by: 1/2029 64250241ALECH Enjoy by: 1/2029
    Where it was sold
    Distributed nationwide
    Amount recalled
    Alehouse Clam Chowder = 5,368 pouches
    Status
    Ended Jun 11, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0685-2025
  10. ENDEDClass II ยท ModerateRecalled Mar 13, 2025

    Tortilla Chip Green 4 cut packed 5lbs per bag; 6 bags per box

    Undeclared Yellow #5

    La Mexicana Tortilla Factory, Inc. ยท Duncanville, TX

    Where it was sold: Texas

    Show details
    Product, as FDA describes it
    Tortilla Chip Green 4 cut packed 5lbs per bag; 6 bags per box
    Reason, in FDA's words
    Undeclared Yellow #5
    Codes on the package
    25072-4
    Where it was sold
    Texas
    Amount recalled
    3 boxes
    Status
    Ended Sep 11, 2026 (FDA lists it as terminated)
    FDA recall number
    F-0715-2025
  11. ENDEDClass II ยท ModerateRecalled Mar 12, 2025

    emd Oysterettes (oyster crackers in polypropylene film). 0.75 oz. Packed for and Distributed by e...

    Foreign object (metal)

    Dairy State Foods Inc ยท Milwaukee, WI

    Where it was sold: MI

    Show details
    Product, as FDA describes it
    emd Oysterettes (oyster crackers in polypropylene film). 0.75 oz. Packed for and Distributed by emd, Detroit, MI 48212.
    Reason, in FDA's words
    Foreign object (metal)
    Codes on the package
    Date Codes: 34824 and 35324
    Where it was sold
    MI
    Amount recalled
    1080 cases (Each case contains Approx 150 units. Case sold by volume of 7 lbs./case)
    Status
    Ended Mar 20, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0642-2025
  12. ENDEDClass II ยท ModerateRecalled Mar 12, 2025

    Julie's Gorditas De Nata; Ingredients: Flour, Vegetable Oil, Sugar, Baking Soda, Milk, Sour Cream, B...

    undeclared allergen ingredient (wheat) on product label for flour Gorditas.

    Julie's Gorditas ยท Pomona, CA

    Where it was sold: Product was sold to two(2) distributors.

    UPC 000202120186
    Show details
    Product, as FDA describes it
    Julie's Gorditas De Nata; Ingredients: Flour, Vegetable Oil, Sugar, Baking Soda, Milk, Sour Cream, Butter, Cream Of Milk, Cinnamon, Vanilla; Net Wt. 16.75 OZ UPC# 0 00202 12018 6
    Reason, in FDA's words
    undeclared allergen ingredient (wheat) on product label for flour Gorditas.
    Codes on the package
    no best by date or lot code applied to product.
    Where it was sold
    Product was sold to two(2) distributors.
    Amount recalled
    240 units
    Status
    Ended Aug 13, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0687-2025
  13. ENDEDClass II ยท ModerateRecalled Mar 12, 2025

    Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. U...

    elevated level of lead

    FRUSELVA USA ยท Miami, FL

    Where it was sold: Nationwide

    UPC 191907993141
    Show details
    Product, as FDA describes it
    Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombia
    Reason, in FDA's words
    elevated level of lead
    Codes on the package
    Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
    Where it was sold
    Nationwide
    Amount recalled
    25,600 units
    Status
    Ended May 7, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0693-2025
  14. ENDEDClass I ยท Most seriousRecalled Mar 11, 2025

    Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook thr...

    Contaminated with Listeria monocytogenes

    New Age International, Inc. ยท Brooklyn, NY

    Where it was sold: Distributed to wholesalers in NY that distributed to other states.

    UPC 8809159458890
    Show details
    Product, as FDA describes it
    Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through before
    Reason, in FDA's words
    Contaminated with Listeria monocytogenes
    Codes on the package
    UPC: 8809159458890
    Where it was sold
    Distributed to wholesalers in NY that distributed to other states.
    Amount recalled
    2720 boxes
    Status
    Ended Aug 7, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0646-2025
  15. ENDEDClass I ยท Most seriousRecalled Mar 11, 2025

    365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482...

    Undeclared allergen (eggs) and pork

    C.H. Guenther & Son LLC ยท San Antonio, TX

    Where it was sold: Nationwide

    UPC 994824997090
    Show details
    Product, as FDA describes it
    365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed by: Whole Foods Market, Austin, TX
    Reason, in FDA's words
    Undeclared allergen (eggs) and pork
    Codes on the package
    Best-By Date: 11/29/25
    Where it was sold
    Nationwide
    Amount recalled
    1818 cases
    Status
    Ended Jun 3, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0702-2025
  16. ENDEDClass III ยท Low riskRecalled Mar 11, 2025

    Farmer House Preserve Olive Strips

    Contains Cyclamates

    Lins Waha International Corp ยท Amityville, NY

    Where it was sold: AL,FL,GA,IL,IN,KS,MA,MD,MI,NC,NJ,NY,OH,OK,PA,TX,VA,WI

    Show details
    Product, as FDA describes it
    Farmer House Preserve Olive Strips
    Reason, in FDA's words
    Contains Cyclamates
    Codes on the package
    Exp Sep. 29. 2025
    Where it was sold
    AL,FL,GA,IL,IN,KS,MA,MD,MI,NC,NJ,NY,OH,OK,PA,TX,VA,WI
    Amount recalled
    178 Cases
    Status
    Ended Feb 3, 2026 (FDA lists it as terminated)
    FDA recall number
    F-0703-2025
  17. ENDEDClass II ยท ModerateRecalled Mar 10, 2025

    Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per d...

    Levels of iodine exceeding label claim

    Veridance Pharmacal, LLC ยท Springdale, AR

    Where it was sold: One customer located in Gladstone, MO

    UPC 850038221294
    Show details
    Product, as FDA describes it
    Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distributed by: McDonagh Medical Center Gladstone, MO 64119
    Reason, in FDA's words
    Levels of iodine exceeding label claim
    Codes on the package
    UPC: 850038221294, Lot codes: 0311-01 exp. 3/26, 0311-02 exp. 3/26, 0367-01 exp. 8/26
    Where it was sold
    One customer located in Gladstone, MO
    Amount recalled
    450 bottles
    Status
    Ended Apr 4, 2025 (FDA lists it as terminated)
    FDA recall number
    F-0671-2025
  18. ENDEDClass I ยท Most seriousRecalled Mar 10, 2025

    Zaarah Herbals brand Bhringraj Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 9997...

    Products contain elevated levels of Lead (Pb): 3.231 ppm and Arsenic (As): 0.958 ppm;

    NEW YORK WHOLESALE GROUP ยท Hicksville, NY

    Where it was sold: NY, CT, NJ, CA

    UPC 635028999731
    Show details
    Product, as FDA describes it
    Zaarah Herbals brand Bhringraj Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99973 1
    Reason, in FDA's words
    Products contain elevated levels of Lead (Pb): 3.231 ppm and Arsenic (As): 0.958 ppm;
    Codes on the package
    Batch No: BJ 04 Mfd. Date: July / 2022
    Where it was sold
    NY, CT, NJ, CA
    Amount recalled
    46.98 cases total
    Status
    Ended Jul 21, 2026 (FDA lists it as terminated)
    FDA recall number
    F-0721-2025
  19. ENDEDClass I ยท Most seriousRecalled Mar 10, 2025

    Zaarah Herbals brand Gurmar Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99969 4

    Products contain elevated levels of Lead (Pb): 3.688 ppm

    NEW YORK WHOLESALE GROUP ยท Hicksville, NY

    Where it was sold: NY, CT, NJ, CA

    UPC 635028999694
    Show details
    Product, as FDA describes it
    Zaarah Herbals brand Gurmar Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99969 4
    Reason, in FDA's words
    Products contain elevated levels of Lead (Pb): 3.688 ppm
    Codes on the package
    Batch No: GD 04 Mfd. Date: July / 2022
    Where it was sold
    NY, CT, NJ, CA
    Amount recalled
    46.98 cases total
    Status
    Ended Jul 21, 2026 (FDA lists it as terminated)
    FDA recall number
    F-0722-2025
  20. ENDEDClass I ยท Most seriousRecalled Mar 10, 2025

    Zaarah Herbals brand Vasaka Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99967 0

    Products contain elevated levels of Lead (Pb): 6.504 ppm

    NEW YORK WHOLESALE GROUP ยท Hicksville, NY

    Where it was sold: NY, CT, NJ, CA

    UPC 635028999670
    Show details
    Product, as FDA describes it
    Zaarah Herbals brand Vasaka Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99967 0
    Reason, in FDA's words
    Products contain elevated levels of Lead (Pb): 6.504 ppm
    Codes on the package
    Batch No: VK 04 Mfd. Date: July / 2022
    Where it was sold
    NY, CT, NJ, CA
    Amount recalled
    46.98 cases total
    Status
    Ended Jul 21, 2026 (FDA lists it as terminated)
    FDA recall number
    F-0723-2025

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What the classes mean

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

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

Class III ยท 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.