The Recall Desk

State

New York product recalls

73,737 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,955
Critical
1,508
Severe
3,701
Most recent
2026-10-28

Of the 12,955 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,701 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32376–32400 of 86692

  • ModerateFDA (Food)·F-1475-2020·2020-09-09

    Sundial White Pond Lily Herbal Product Recalled for Misbranding

    Sundial Herbal Products is recalling White Pond Lily herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***WHITE POND LILY***1oz.***USES: CANCER, DOUCHE, TUBERCULOSIS IN LYMPH GLANDS, GONORRHEA, ULCER IN MOUTH & THROAT***"; packaged in clear plastic zip-top bags
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1496-2020·2020-09-09

    Sundial Herbal Worms and Parasites Formula Recalled as Unapproved Drug

    Sundial Herbal Products is recalling its Traditional Herbal Formula for Worms & Parasites because the product is misbranded and deemed an unapproved drug.

    Product
    "SUNDIAL***TRADITIONAL HERBAL FORMULA***Worms & Parasites***" packaged in boxes
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2931-2020·2020-09-09

    Stimwave StimQ Peripheral Nerve Stimulator System Recalled for Non-Functional Component

    Stimwave Technologies is recalling six StimQ Peripheral Nerve Stimulator Systems because they contain a non-functional component not referenced in product labeling.

    Product
    StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1557-2020·2020-09-09

    Santa Cruz Recalls Subpotent UltraCruz Hand Sanitizing Gel

    Santa Cruz Biotechnology is recalling 14,238 bottles of UltraCruz Hand Sanitizing Gel because the product is subpotent.

    Product
    UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol), packaged in 3 Fluid Oz./89 mL bottes, Manufactured By Santa Cruz Biotechnology, Inc. 10410 Finnell St. Dallas, TX 75220
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1494-2020·2020-09-09

    Sundial Herbal Blood Pressure Formula Recalled for Misbranding and Unapproved Drug Status

    Sundial Herbal Products is recalling Sundial Traditional Herbal Formula Blood Pressure boxes under a permanent injunction. The products are misbranded and deemed unapproved drugs due to labeling claims.

    Product
    "SUNDIAL***TRADITIONAL HERBAL FORMULA***BLOOD PRESSURE***" packaged in boxes
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1491-2020·2020-09-09

    Sundial African Manback Tonic Recalled for Misbranding and Unapproved Drug Claims

    Sundial Herbal Products is recalling Sundial Traditional African Manback Tonic because the product is misbranded and deemed an unapproved drug based on its labeling claims.

    Product
    "SUNDIAL***TRADITIONAL AFRICAN MANBACK TONIC***remember the strength of the reproductive organ, reflects the strength of the entire body. Take SUNDIAL AFRICAN MANBACK TONIC to strengthen, rejuvenate & energize***" packaged in glass bottles
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1458-2020·2020-09-09

    Sundial Herbal Products Recalls Misbranded Sarsaparilla Herbal Product

    Sundial Herbal Products is recalling Sarsaparilla herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***SARSAPARILLA***2 oz.***USES: BLOOD CLEANSER, BALANCES HORMONES, PRODUCTIVE ORGANS, SYPHILIS, ECZEMA, PSORIASIS***"; packaged in clear plastic zip-top bags.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1451-2020·2020-09-09

    Sundial Herbal Products Recalls Cerasee Herbal Product for Misbranding

    Sundial Herbal Products is recalling Cerasee herbal products under a permanent injunction because the items are misbranded and considered unapproved drugs.

    Product
    "SUNDIAL Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***CERASEE***1 oz.***USES: DIABETES, HYPERTENSION, WORMS, DYSENTERY, MALARIA, BLOOD PURIFIER"; packaged in clear zip-top bags
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1478-2020·2020-09-09

    Sundial Trumpet Leaf Herbal Product Recalled for Misbranding and Unapproved Drug Claims

    Sundial Herbal Products is recalling Trumpet Leaf herbal products under a permanent injunction because the items are misbranded and deemed unapproved drugs based on labeling claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***TRUMPET LEAF***1 oz.***USES: DIABETES, ASTHMA, CONGESTION, SKIN BATH, ULCERS, SORES, PARKINSON'S DISEASE, KIDNEY***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2914-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect could cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1460-2020·2020-09-09

    Sundial Sea Moss Recalled for Unapproved Drug Claims

    Sundial Herbal Products is recalling Sea Moss/Irish Moss products because they are misbranded and deemed unapproved drugs based on labeling claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERB***SEA MOSS/IRISH MOSS***2oz.***USES: IODINE, BREAKS UP FAT & MUCOUS, ADD, ULCERS, CALCIUM, THYROID, DETOX***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1446-2020·2020-09-09

    Sundial Herbal Products Recalls Jamaican Bissy Powder for Unapproved Drug Claims

    Sundial Herbal Products is recalling Jamaican Bissy Powder because the product is misbranded and deemed an unapproved drug based on its labeling claims.

    Product
    Jamaican Bissy Powder; "***Bissy regulates the heart, removes and prevents water from settling around the heart, lessens the desire for drugs, cigarettes, alcohol by clearing the body and blood of poison viruses & toxins etc. Relieves fatigue gives stamina and endurance enabling…
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1500-2020·2020-09-09

    Sundial Cassava Meal Recalled as Unapproved Drug

    Sundial Herbal Products is recalling Sundial Cassava Meal because the product is misbranded and deemed an unapproved drug based on its labeling claims.

    Product
    "SUNDIAL***CASSAVA MEAL***" packaged in brown bags with a clear viewing window
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1477-2020·2020-09-09

    Sundial Quassia Wood Recalled for Unapproved Drug Claims

    Sundial Herbal Products is recalling Quassia Wood under a court order because the product is misbranded and considered an unapproved drug due to its labeling.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***QUASSIA WOOD***2 oz.***USES: ALCOHOLISM, LIVER, STOMACH COMPLAINTS, DIGESTIVE SYSTEM, KILLS LICE & PARASITES***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1453-2020·2020-09-09

    Sundial Mango Bark Herbal Product Recalled for Unapproved Drug Claims

    Sundial Herbal Products is recalling Mango Bark herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***MANGO BARK***2 oz.***USES: KIDNEY STONE, HIGH BLOOD PRESSURE, RELATED TO NERVOUS CONDITIONS***"
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1448-2020·2020-09-09

    Sundial Herbal Products Recalls Mitmitta Cayenne Pepper Product

    Sundial Herbal Products is recalling Mitmitta (Cayenne Pepper) because it is misbranded and deemed an unapproved drug due to labeling claims.

    Product
    Mitmitta (Cayenne Pepper); "Traditional Uses: Prevents heart attacks, and lowers high blood pressure, stops internal bleeding, Heals ulcers and pains there of: Improves circulation, thins blood and keeps it moving***"
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1495-2020·2020-09-09

    Sundial Traditional Herbal Formula Heart Recalled for Misbranding

    Sundial Herbal Products is recalling its Traditional Herbal Formula Heart product because it is misbranded and deemed an unapproved drug.

    Product
    "SUNDIAL***TRADITIONAL HERBAL FORMULA***HEART***" packaged in boxes
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1482-2020·2020-09-09

    Sundial Guava Leaf Herbal Product Recalled for Unapproved Drug Claims

    Sundial Herbal Products is recalling Guava Leaf herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***GUAVA LEAF***1oz.***USES: BLOOD PRESSURE, WORMS, NERVES, DIABETES***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1364-2020·2020-09-09

    Newman's Own Organic Decaf Coffee Recalled for Containing Non-Organic Beans

    Keurig Dr Pepper is recalling Newman's Own Organic Decaf Ground Coffee because it contains regular non-organic coffee. Consumers should stop using the product.

    Product
    Newman's Own Organics, Newman's Special Decaf Medium Roast, Ground Coffee, 10 oz.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1481-2020·2020-09-09

    Sundial Herbal Products Recalls Guinea Hen Weed for Unapproved Drug Claims

    Sundial Herbal Products is recalling Guinea Hen Weed herbal products under a permanent injunction because the labeling makes unapproved drug claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***GUINEA HEN WEED***1 oz.***USES: ARTHRITIS, RHEUMATISM, STIMULATE IMMUNE SYSTEM, FIGHTS CANCER CELLS, VIRUSES, YEAST***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1462-2020·2020-09-09

    Sundial Black Sage Herbal Product Recalled for Unapproved Drug Claims

    Sundial Herbal Products is recalling Black Sage herbal products under a permanent injunction because the labeling makes unapproved drug claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BLACK SAGE***1 oz.***USES: ALZHEIMER'S DISEASE, GINGIVITIS, MENOPAUSE, APPLY DIRECTLY TO SKIN FOR COLD SORES, ASTHMA***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1488-2020·2020-09-09

    Sundial Wood and Root Tonic Recalled for Misbranding and Unapproved Drug Claims

    Sundial Herbal Products is recalling Wood and Root Tonic under a permanent injunction because the product is misbranded and deemed an unapproved drug.

    Product
    "Sundial***Traditional Jamaican***ORGANIC***Original Maroon Recipe***WOOD AND ROOT TONIC***used for centuries in Jamaica as a household remedy, to cleanse the body and the blood of mucus, and toxic waste.***used by the Carib Indians of Central America to Protect them against…
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1484-2020·2020-09-09

    Sundial King of the Forest Herbal Product Recalled for Misbranding

    Sundial Herbal Products is recalling King of the Forest herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***KING OF THE FOREST***1 oz.***USES: HYPERTENSION, ASTHMA, THROAT, KIDNEY, LIVER SPOTS, HERPES RASHES***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state