The Recall Desk

Hazard

Cgmp Deviation recalls

1,563 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,563
Critical
1
Severe
288
Most recent
2026-09-09

Of the 1,563 cgmp deviation recalls we have scored against our rubric, 1 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 288 (18%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all cgmp deviation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1126–1150 of 1563

  • ModerateFDA (Drugs)·D-1587-2019·2019-08-14

    Herbal Doctor Remedies Recalls Asma Aid Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Asma Aid because it was manufactured outside of required Good Manufacturing Practices. The product was distributed nationwide and in Brazil.

    Product
    Asma Aid Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1595-2019·2019-08-14

    Dragon Pain Oil Recalled for Manufacturing Process Deviations

    Herbal Doctor Remedies is recalling Dragon Pain Oil because it was manufactured outside of required Good Manufacturing Practices controls.

    Product
    Dragon Pain Oil, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1618-2019·2019-08-14

    Herbal Doctor Remedies Recalls Thyro-H Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Thyro-H 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.

    Product
    Thyro-H, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1622-2019·2019-08-14

    Herbal Doctor Remedies Recalls Detensin Capsules Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Detensin 500 mg capsules because they were manufactured outside of current Good Manufacturing Practice controls.

    Product
    Detensin, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1624-2019·2019-08-14

    Herbal Doctor Remedies Recalls Thyro-Lo Capsules Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Thyro-Lo 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Thyro-Lo, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1612-2019·2019-08-14

    Herbal Doctor Remedies Recalls Pain Stopper Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Pain Stopper 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1591-2019·2019-08-14

    Herbal Doctor Remedies Recalls Bone Fixer Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Bone Fixer because it was manufactured outside of required Good Manufacturing Practices controls.

    Product
    Bone Fixer, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1610-2019·2019-08-14

    Herbal Doctor Remedies Recalls Migraine Off Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Migraine Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Migraine Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1626-2019·2019-08-14

    Herbal Doctor Remedies Recalls Appetrol Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Appetrol Capsules because they were manufactured outside of current Good Manufacturing Practice controls.

    Product
    Appetrol Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1613-2019·2019-08-14

    Herbal Doctor Remedies Recalls Prostatin Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Prostatin Capsules because they were manufactured outside of current Good Manufacturing Practice controls.

    Product
    Prostatin Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1611-2019·2019-08-14

    Herbal Doctor Remedies Recalls Pain Away Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Pain Away 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices.

    Product
    Pain Away, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1603-2019·2019-08-14

    Herbal Doctor Remedies Recalls Herpes-V Balm for Manufacturing Violations

    Herbal Doctor Remedies is recalling Herpes-V Balm because it was manufactured outside of required Good Manufacturing Practices controls.

    Product
    Herpes-V Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1629-2019·2019-08-14

    Herbal Doctor Remedies Recalls Fungo Off Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Fungo Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Fungo Off Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1594-2019·2019-08-14

    Dragon Pain Balm Recalled for CGMP Manufacturing Deviations

    Herbal Doctor Remedies is recalling Dragon Pain Balm because it was manufactured outside of current Good Manufacturing Practices controls.

    Product
    Dragon Pain Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1628-2019·2019-08-14

    Herbal Doctor Remedies Recalls Asma Stopper Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Asma Stopper Capsules because they were manufactured outside of current Good Manufacturing Practice controls.

    Product
    Asma Stopper Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1547-2019·2019-08-07

    NingBo Huize Recalls Pink Lemonade Hand Gel for Missing Stability Testing

    NingBo Huize Commodity Co., Ltd. is recalling 20,160 units of Pink Lemonade Scented Antibacterial Hand Gel because stability testing was not conducted.

    Product
    AMERICA'S ORIGINAL DUBBLE BUBBLE Pink Lemonade SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1535-2019·2019-08-07

    Tootsie Roll Antibacterial Hand Gel Recalled for Missing Stability Testing

    NingBo Huize Commodity Co., Ltd. is recalling Tootsie Roll POP Orange Scented Antibacterial Hand Gel because stability testing was not conducted.

    Product
    Tootsie Roll POP ORANGE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1557-2019·2019-08-07

    Recall of ICEE Peach Scented Antibacterial Hand Gel for CGMP Deviations

    NingBo Huize Commodity Co., Ltd. is recalling ICEE Peach Scented Antibacterial Hand Gel because stability testing was not conducted on the product.

    Product
    ICEE PEACH SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1540-2019·2019-08-07

    NingBo Huize Recalls Dots Scented Antibacterial Hand Gel for CGMP Deviations

    NingBo Huize Commodity Co., Ltd. is recalling Dots Scented Antibacterial Hand Gel because stability testing was not conducted on the product.

    Product
    DOTS SCENTED ANTIBACTERIAL HAND GEL STRAWBRRY (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1536-2019·2019-08-07

    Tootsie Roll Antibacterial Hand Gel Recalled for Missing Stability Testing

    NingBo Huize Commodity Co., Ltd. is recalling Tootsie Roll POP Chocolate Scented Antibacterial Hand Gel because stability testing was not conducted.

    Product
    Tootsie Roll POP CHOCOLATE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1538-2019·2019-08-07

    DOTS Scented Antibacterial Hand Gel Recalled for Stability Testing Deviations

    NingBo Huize Commodity Co., Ltd. is recalling DOTS Scented Antibacterial Hand Gel Orange because stability testing was not conducted on the product.

    Product
    DOTS SCENTED ANTIBACTERIAL HAND GEL ORANGE (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1534-2019·2019-08-07

    Hand Sanitizer Recalled for Missing Stability Testing

    NingBo Huize Commodity Co., Ltd. is recalling 50,000 units of hand sanitizer because stability testing was not conducted.

    Product
    Texas Home Health Home Care Hospice Personal Care Hand Sanitizer (Ethyl Alcohol 62%), 0.33 oz/10 mL, OTC, Made in China
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1532-2019·2019-08-07

    NingBo Huize Recalls SPF 30 Sunscreen Lotion Due to Missing Stability Testing

    NingBo Huize Commodity Co., Ltd. is recalling SPF 30 Sunscreen Lotion because stability testing was not conducted on the manufactured product.

    Product
    SPF 30 SUNSCREEN LOTION Active Ingredients Octinoxate 7.5%, Octisalate 2.0%, Oxybenzone 4.0% Titanium Dioxide 2.5% Sunscreen, 53mL/1.8fl.oz., OTC, Distributed by: EVANS, Made in China
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1563-2019·2019-08-07

    NingBo Huize Recalls Dippin' Dots Hand Gel Due to Missing Stability Testing

    NingBo Huize is recalling Dippin' Dots Scented Cotton Candy Antibacterial Hand Gel because stability testing was not conducted on the product.

    Product
    DIPPIN' DOTS SCENTED COTTON CANDY ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1555-2019·2019-08-07

    NingBo Huize Recalls Air Heads Hand Gel for Missing Stability Testing

    NingBo Huize Commodity Co., Ltd. is recalling Air Heads Orange Scented Antibacterial Hand Gel because stability testing was not conducted on the product.

    Product
    AIR HEADS ORANGE SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
    Category
    Drug
    Distribution
    0 states