The Recall Desk

Hazard

Cgmp Violation recalls

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

What the numbers show

Total
108
Critical
0
Severe
3
Most recent
2026-07-08

Of the 108 cgmp violation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (3%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all cgmp violation 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.

101–108 of 108

  • ModerateFDA (Drugs)·D-1494-2019·2019-07-31

    Pharma-Natural Recalls Army Health Pain Reliever Roll-On for CGMP Violations

    Pharma-Natural Inc. is recalling Army Health Pain Reliever Roll-On bottles due to manufacturing process violations. The product was distributed in Florida and Texas.

    Product
    ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On, 2.5 FL OZ (73ML) roll on bottle, Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00408 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1496-2019·2019-07-31

    Pharma-Natural Recalls Army Health Pain Reliever Gel Due to CGMP Violations

    Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.

    Product
    ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%), 0.5 OZ jar, Manufactured exclusively for: Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00461 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1501-2019·2019-07-31

    Lido E.R. Lidocaine Cream Recalled for Manufacturing Violations

    Pharma-Natural Inc. is recalling Lido E.R. Lidocaine Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.

    Product
    Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream, 4 oz (113 g) jar, Distributed by Diabetic Supply of Suncoast, Inc., P.O. Box 2102, Vega Alta, PR 00692, NDC 63788-115-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1492-2019·2019-07-31

    Pharma-Natural Recalls Oliver's Harvest CBD+Capsaicin Cream for CGMP Violations

    Pharma-Natural Inc. is recalling 998 bottles of Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief Cream due to current good manufacturing practice violations.

    Product
    Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief (Capsaicin 0.2%) Topical Analgesic Cream, 4 OZ (113.4 g) bottle with pump, Distributed by: Coast to Coast Natural, Inc., Wellington, FL 33414, NDC 63788-120-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2019·2018-10-17

    Pfizer Recalls Glipizide XL Tablets Due to Manufacturing Deviations

    Pfizer is recalling 7,777 bottles of Glipizide XL 5 mg tablets because rejected product was used in manufacturing, violating CGMP standards.

    Product
    Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-3356-2017·2017-08-16

    Duy Drugs Recalls Cardiovid Plus Dietary Supplement for CGMP Violations

    Duy Drugs Inc. is recalling 411 bottles of Cardiovid Plus dietary supplements because they failed to meet FDA current good manufacturing practice requirements.

    Product
    Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-3355-2017·2017-08-16

    Duy Drugs Recalls Viva ben Femenine Supplement for CGMP Violations

    Duy Drugs Inc. is recalling 1,800 bottles of Viva ben Femenine Supplement because the product failed to meet current good manufacturing practices (CGMPs) for identity, purity, and composition.

    Product
    Viva ben Femenine Supplement, Dietary Supplement 30 Softgels
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1992-2014·2014-07-16

    Amerigel Wound Dressing Recalled for Manufacturing Process Concerns

    Kova Laboratories is recalling Amerigel Wound Dressing 1 oz. tubes because they may not have been manufactured pursuant to a validated process protocol and CGMP.

    Product
    Amerigel Wound Dressing 1 oz. tube
    Category
    Medical Device
    Distribution
    2 states