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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

28,406 ended recalls · showing 1,061 to 1,080

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  1. ENDEDClass II · ModerateRecalled Jun 24, 2025

    Fresh Scottish Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 ...

    RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products ...

    Moon N Sea GA LLC · Buford, GA

    Where it was sold: Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from...

    Show details
    Product, as FDA describes it
    Fresh Scottish Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 fillets per box). Boxes contain ice for temperature control. Keep Refrigerated.
    Reason, in FDA's words
    RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
    Codes on the package
    No printed expiration dates all products were delivered fresh within 1~2 days of processing
    Where it was sold
    Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from the firm.
    Amount recalled
    1429.13 lb
    Status
    Ended Aug 5, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0351-2025
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Jun 24, 2025

    Blue Fin Tuna, Net WT (variable weight) 50 lb brown corrugated carboard box. Boxes contain ice for t...

    RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products ...

    Moon N Sea GA LLC · Buford, GA

    Where it was sold: Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from...

    Show details
    Product, as FDA describes it
    Blue Fin Tuna, Net WT (variable weight) 50 lb brown corrugated carboard box. Boxes contain ice for temperature control. Keep Refrigerated.
    Reason, in FDA's words
    RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
    Codes on the package
    No printed expiration dates all products were delivered fresh within 1~2 days of processing
    Where it was sold
    Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from the firm.
    Amount recalled
    59 lb
    Status
    Ended Aug 5, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0352-2025
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jun 24, 2025

    Yellow Fin Tuna, Net WT (variable weight) 50 lb brown corrugated carboard box. Boxes contain ice for...

    RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products ...

    Moon N Sea GA LLC · Buford, GA

    Where it was sold: Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from...

    Show details
    Product, as FDA describes it
    Yellow Fin Tuna, Net WT (variable weight) 50 lb brown corrugated carboard box. Boxes contain ice for temperature control. Keep Refrigerated.
    Reason, in FDA's words
    RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
    Codes on the package
    No printed expiration dates all products were delivered fresh within 1~2 days of processing
    Where it was sold
    Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from the firm.
    Amount recalled
    68.10 lb
    Status
    Ended Aug 5, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0353-2025
    View in FDA's recall database
  4. ENDEDClass III · Low riskRecalled Jun 24, 2025

    a.) Actylis brand Lithium Orotate 4% packaged in HDPE Liner in a 25kg carton b.) Actylis brand Lith...

    4% Lithium Orotate product may only contain 3% and 9% Lithium Orotate product may contain 4.45%

    Aceto US, L.L.C · Port Washington, NY

    Where it was sold: NJ, NC, CA, UT, MT, FL, AZ, NC, NY

    Show details
    Product, as FDA describes it
    a.) Actylis brand Lithium Orotate 4% packaged in HDPE Liner in a 25kg carton b.) Actylis brand Lithium Orotate 9% packaged in HDPE Liner in a 25kg carton
    Reason, in FDA's words
    4% Lithium Orotate product may only contain 3% and 9% Lithium Orotate product may contain 4.45%
    Codes on the package
    a.) SKU: TLIOR0104 and Lot Numbers: T250464; T250265; T250184; T240967; T240619; T240452; T240346; T230944; T20230304 b.) SKU: TLIOR0109 and Lot Numbers: T250409; T250353; T250310; T250124; T241240; T240936; T240560; T240125; T20230223; T20230403; T20220701; T20221002; T20221204
    Where it was sold
    NJ, NC, CA, UT, MT, FL, AZ, NC, NY
    Amount recalled
    9%: 6033.45 Kg; 4%: 4485.95 Kg
    Status
    Ended Jul 31, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0441-2025
    View in FDA's recall database
  5. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate, 1MG, Distributed by Enjoy Nutrition, LLC. UPC#: 717340952714

    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

    Enjoy Nutrition, LLC; dba Weyland Brain Nutrition · San Francisco, CA

    Where it was sold: Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide

    UPC 717340952714
    Show details
    Product, as FDA describes it
    Lithium Orotate, 1MG, Distributed by Enjoy Nutrition, LLC. UPC#: 717340952714
    Reason, in FDA's words
    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
    Codes on the package
    Lot#: 21442; 22647
    Where it was sold
    Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide
    Amount recalled
    159,926 units across all product sizes
    Status
    Ended Mar 25, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0442-2025
    View in FDA's recall database
  6. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate, 2.5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 719318414002; 709750005289

    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

    Enjoy Nutrition, LLC; dba Weyland Brain Nutrition · San Francisco, CA

    Where it was sold: Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide

    UPC 719318414002UPC 709750005289
    Show details
    Product, as FDA describes it
    Lithium Orotate, 2.5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 719318414002; 709750005289
    Reason, in FDA's words
    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
    Codes on the package
    Lot#: 21166; 21640; 21821; 22281; 22757
    Where it was sold
    Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide
    Amount recalled
    159,926 units across all product sizes
    Status
    Ended Mar 25, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0443-2025
    View in FDA's recall database
  7. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate, 5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730893968, 702730894064

    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

    Enjoy Nutrition, LLC; dba Weyland Brain Nutrition · San Francisco, CA

    Where it was sold: Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide

    UPC 702730893968UPC 702730894064
    Show details
    Product, as FDA describes it
    Lithium Orotate, 5MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730893968, 702730894064
    Reason, in FDA's words
    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
    Codes on the package
    Lot#: 21123; 21300; 21498; 21783; 21994; 22218; 22299; 22457; 22718; 23014
    Where it was sold
    Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide
    Amount recalled
    159,926 units across all product sizes
    Status
    Ended Mar 25, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0444-2025
    View in FDA's recall database
  8. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate, 10MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730894033, 702730894057

    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

    Enjoy Nutrition, LLC; dba Weyland Brain Nutrition · San Francisco, CA

    Where it was sold: Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide

    UPC 702730894033UPC 702730894057
    Show details
    Product, as FDA describes it
    Lithium Orotate, 10MG, Distributed by Enjoy Nutrition, LLC. UPC#: 702730894033, 702730894057
    Reason, in FDA's words
    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
    Codes on the package
    Lot#: 21107; 21181; 21288; 21371; 21499; 21695; 21993; 22105; 22200; 22399; 22556; 22650; 22736; 23015; 23016
    Where it was sold
    Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide
    Amount recalled
    159,926 units across all product sizes
    Status
    Ended Mar 25, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0445-2025
    View in FDA's recall database
  9. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate, 20MG, Distributed by Enjoy Nutrition, LLC. UPC#: none

    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.

    Enjoy Nutrition, LLC; dba Weyland Brain Nutrition · San Francisco, CA

    Where it was sold: Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide

    Show details
    Product, as FDA describes it
    Lithium Orotate, 20MG, Distributed by Enjoy Nutrition, LLC. UPC#: none
    Reason, in FDA's words
    Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
    Codes on the package
    Lot#: 2130; 21505; 21911; 22106; 22257; 22397; 22557; 22918; 23035
    Where it was sold
    Distribution includes Amazon, Excel 3PL and Encore Fulfillment. Nationwide
    Amount recalled
    159,926 units across all product sizes
    Status
    Ended Mar 25, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0446-2025
    View in FDA's recall database
  10. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutt...

    Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.

    GMP Laboratories of America Inc · Anaheim, CA

    Where it was sold: Distribution was to a single customer who received product in California and Oklahoma.

    Show details
    Product, as FDA describes it
    Lithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 Sutter St., Suite 405, San Fransisco, CA 94108 2.5 mg UPC#: X002T4OPLL 10 mg UPC#: X0031AXVE9
    Reason, in FDA's words
    Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
    Codes on the package
    2.5mg Lot #: 21822 Expire date: 09/2026 10mg Lot#: 21108; 22649 Expire date: 10/2025; 01/2028
    Where it was sold
    Distribution was to a single customer who received product in California and Oklahoma.
    Amount recalled
    ~185,482 capsules
    Status
    Ended Feb 24, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0447-2025
    View in FDA's recall database
  11. ENDEDClass III · Low riskRecalled Jun 24, 2025

    Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed b...

    Downstream recall of a dietary supplement ingredient that was manufactured out of specification.

    GMP Laboratories of America Inc · Anaheim, CA

    Where it was sold: Distribution was to a single customer who received product in California and Oklahoma.

    Show details
    Product, as FDA describes it
    Lithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed by Enjoy Nutirtion, LLC. San Francisco, CA 94108, (415) 894-0537 2.5 mg UPC#: X001SBI13J 5 mg UPC#: X000PY16Z5 10 mg UPC#: X000T9B9B7 20 mg UPC#: X001VBLW8H 1000 MCG UPC#: X003SBV661
    Reason, in FDA's words
    Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
    Codes on the package
    2.5mg Lot #: 21166, 21640, 21821, 22281, 22757 Expire date: 11/2025, 09/2026, 05/2027, 02/2028 5 mg Lot#: 21123, 21300, 21498, 21783, 21994, 22218, 22299, 22457, 22718 Expire date: 10/2025, 05/2026, 08/2026, 01/2027, 04/2027, 05/2027, 08/2027, 02/2028 10mg Lot#: 21107, 21181, 21288, 21371, 21499, 21695, 21993, 22105, 22200, 22399, 22556, 22650, 22736 Expire date: 10/2025, 12/2025, 02/2026, 03/2026, 05/2026, 07/2026, 01/2027, 01/2027, 03/2027, 07/2027, 10/2027, 01/2028, 02/2029 20mg Lot#: 21301, 21505, 21911, 22106, 22257, 22397, 22557, 22918 Expire date: 02/2026, 05/2026, 10/2026, 05/2027, 07/2028, 10/2027, 04/2028 1000 MCG Lot#: 21442, 22647 Expire date: 05/2025, 01/2027
    Where it was sold
    Distribution was to a single customer who received product in California and Oklahoma.
    Amount recalled
    ~185,482 capsules
    Status
    Ended Feb 24, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0448-2025
    View in FDA's recall database
  12. ENDEDClass III · Low riskRecalled Jun 23, 2025

    Pasteurized Donor Human Milk , 4oz plastic bottle

    Foreign material (plastic particulate from outer closure) between immediate closure (foil seal) and outer closure (plastic cap)

    Henry Ford Milk Bank- Jackson · Jackson, MI

    Where it was sold: MI

    Show details
    Product, as FDA describes it
    Pasteurized Donor Human Milk , 4oz plastic bottle
    Reason, in FDA's words
    Foreign material (plastic particulate from outer closure) between immediate closure (foil seal) and outer closure (plastic cap)
    Codes on the package
    Batch 000230-1, Expiration date 1/5/2026 Batch 000235-1 Expiration date 9/5/2025
    Where it was sold
    MI
    Amount recalled
    209 bottles
    Status
    Ended Sep 9, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0280-2025
    View in FDA's recall database
  13. ENDEDClass III · Low riskRecalled Jun 20, 2025

    New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Number:F03308 UPC:812361033081. Singl...

    Clear coat seal on the lid of the single serve cups did not get applied consistently to all cups in the production run. This resulted in the food safe...

    CinFranky LLC dba New Mexico Pinon Coffee · Albuquerque, NM

    Where it was sold: Nationwide

    UPC 812361033081
    Show details
    Product, as FDA describes it
    New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Number:F03308 UPC:812361033081. Single Serve (Keurig) Cups, filled with ground coffee flavored with natural flavorings.
    Reason, in FDA's words
    Clear coat seal on the lid of the single serve cups did not get applied consistently to all cups in the production run. This resulted in the food safe ink printing on some cups to run when exposed to high temperature, high-pressure water used in a K-cup machine.
    Codes on the package
    Lot Code: 251749 Best Buy Date: 05/08/2026
    Where it was sold
    Nationwide
    Amount recalled
    154 Eaches
    Status
    Ended Aug 11, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0273-2025
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Jun 20, 2025

    Middle East Coast brand Tahini Dip; NET WT: 6 OZ (170g); INGREDIENTS: TAHINI, ORGANIC LEMON JUICE, G...

    Product may be contaminated with spoilage organisms.

    Shovel and Spoon LLC · Limington, ME

    Where it was sold: ME, NH, MA

    UPC 860005502813
    Show details
    Product, as FDA describes it
    Middle East Coast brand Tahini Dip; NET WT: 6 OZ (170g); INGREDIENTS: TAHINI, ORGANIC LEMON JUICE, GARLIC, OLIVE OIL, SEA SALT, ORGANIC TOASTED SESAME. CONTAINS SESAME; Locally Crafted by SHOVEL AND SPOON; UPC 8 60005 50281 3
    Reason, in FDA's words
    Product may be contaminated with spoilage organisms.
    Codes on the package
    MECT1082 Best by: 6/26/25 MECT1083 Best By: 7/3/25
    Where it was sold
    ME, NH, MA
    Amount recalled
    658 tubs
    Status
    Ended Feb 11, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0307-2025
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Jun 19, 2025

    VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup...

    Potential to be contaminated with Listeria monocytogenes

    Face Rock Creamery LLC · Bandon, OR

    Where it was sold: Distributed in CA and OR.

    Show details
    Product, as FDA describes it
    VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup with lid. UPC on 6oz. retail cup: 8 51222 00528 7. FaceRockCreamery.com MASTER CASE's label is read in parts: Item No. 240062 Vampire Slayer Curds 12/6oz., net wt. 4.5 lbs. Face Rock Creamery 680 2nd St. SE Bandon, OR 97411.
    Reason, in FDA's words
    Potential to be contaminated with Listeria monocytogenes
    Codes on the package
    Lot numbers: 20250519VS01 and 20250519VS02. Use By: 08292025 Lot number breaks down as: 2025 = Year 05 = Month 19 = Day of Month VS = Cheese type code 01 or 02 = Production (Vat)
    Where it was sold
    Distributed in CA and OR.
    Amount recalled
    260 cases (12/6oz. cups per case)
    Status
    Ended Nov 26, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0214-2025
    View in FDA's recall database
  16. ENDEDClass III · Low riskRecalled Jun 19, 2025

    SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per case.

    Undeclared Red No. 3 (E127)]

    SHANDONG JOYWIN INTERNATIONAL TRADING CO.,LTD. · Weifang, N/A

    Where it was sold: The recalled product was distributed to the following states: IL, PA, FL, AL

    Show details
    Product, as FDA describes it
    SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per case.
    Reason, in FDA's words
    Undeclared Red No. 3 (E127)]
    Codes on the package
    R241077 Production Code Date: CAN CODE: 3700/01115 Best by: NOV/26/2027 624 R241079 Production Code Date: CAN CODE: 3700/01115 Best by: DEC/04/2027 624
    Where it was sold
    The recalled product was distributed to the following states: IL, PA, FL, AL
    Amount recalled
    1105 Cases
    Status
    Ended Jul 18, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0259-2025
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Jun 18, 2025

    Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Caps...

    Products contains Magnesium Salicylate.

    Professional Botanicals, Inc. · Ogden, UT

    Where it was sold: Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, ...

    Show details
    Product, as FDA describes it
    Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku: PB248
    Reason, in FDA's words
    Products contains Magnesium Salicylate.
    Codes on the package
    Lot #: 71527
    Where it was sold
    Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.
    Amount recalled
    452 Bottles
    Status
    Ended Dec 31, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0181-2026
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Jun 18, 2025

    Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 ...

    Products contains Magnesium Salicylate.

    Professional Botanicals, Inc. · Ogden, UT

    Where it was sold: Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, ...

    Show details
    Product, as FDA describes it
    Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.
    Reason, in FDA's words
    Products contains Magnesium Salicylate.
    Codes on the package
    Lot #: 280914
    Where it was sold
    Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.
    Amount recalled
    430 Bottles
    Status
    Ended Dec 31, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0182-2026
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Jun 18, 2025

    Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsu...

    Products contains Magnesium Salicylate.

    Professional Botanicals, Inc. · Ogden, UT

    Where it was sold: Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, ...

    Show details
    Product, as FDA describes it
    Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
    Reason, in FDA's words
    Products contains Magnesium Salicylate.
    Codes on the package
    Lot #: 290301
    Where it was sold
    Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.
    Amount recalled
    253 Bottles
    Status
    Ended Dec 31, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0183-2026
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Jun 18, 2025

    JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392...

    Undeclared milk

    Lipari Foods Operating Company, LLC. · Warren, MI

    Where it was sold: Nationwide in retail stores

    UPC 760208124501
    Show details
    Product, as FDA describes it
    JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
    Reason, in FDA's words
    Undeclared milk
    Codes on the package
    Lot #'s: 28202501A, 29202501A, 23202504A, 14202505A, 15202505A, 03202506A
    Where it was sold
    Nationwide in retail stores
    Amount recalled
    971 cases
    Status
    Ended Aug 19, 2025 (FDA lists it as terminated)
    FDA recall number
    H-0213-2025
    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.