The Recall Desk

Hazard

Gmp Deviations recalls

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

What the numbers show

Total
5
Critical
0
Severe
3
Most recent
2020-11-25

Of the 5 gmp deviations 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 (60%) 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 gmp deviations 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.

1–5 of 5

  • ModerateFDA (Drugs)·D-0087-2021·2020-11-25

    Milbar Recalls DCL T Shampoo for GMP Deviations

    Milbar Laboratories is voluntarily recalling 1,225 bottles of DCL T Shampoo due to Good Manufacturing Practice (GMP) deviations.

    Product
    DCL T Shampoo for Hair and Body ( Solution Coal Tar U.S.P. 3% and 0.6% Coal Tar), 300 ml/ 10.1 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 3574865069947
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0812-2018·2018-05-23

    Milbar Recalls Solar Defense Sunscreen Due to GMP Deviations

    Milbar Laboratories is recalling 2,156 tubes of Solar Defense Sheer Sunscreen SPF50 due to Good Manufacturing Practice (GMP) deviations.

    Product
    Solar Defense Sheer Sunscreen Broad Spectrum SPF50 (Octinoxate 7.5%, Zinc Oxide 10.5%), 2.5 FL OZ. 74 mL, Distributed by: BeautyRx LLC, NY, NY 10128
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0950-2017·2017-07-12

    Phillips Co. Recalls StingMed Insect Bites Skin Protectant Due to GMP Deviations

    Phillips Co. is recalling StingMed Insect Bites Skin Protectant because FDA inspections found significant manufacturing deviations that raise questions about the product's safety and quality.

    Product
    StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 04307-100-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0949-2017·2017-07-12

    Phillips Recalls Diabecline Topical Ointment Due to Manufacturing Deviations

    Phillips Co. is recalling Diabecline brand Topical Ointment First Aid Antibiotic because FDA inspections found significant manufacturing deviations that question the product's safety and quality.

    Product
    Diabecline brand Topical Ointment First Aid Antibiotic, tetracycline (3%), 3 mL in a 5 mL bottle, sold over the counter Phillips Company, Millerton, OK -- NDC 04307-100-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-053-2013·2012-11-21

    New England Compounding Center Recalls Non-Sterile Products Due to GMP Deviations

    New England Compounding Center is voluntarily recalling all non-sterile products due to Good Manufacturing Practice (GMP) deviations. The recall covers products distributed nationwide and in Japan.

    Product
    All Non Sterile Products manufactured by NECC (New England Compounding Center), Framingham, MA. A complete list of products can be found on their website at www.neccrx.com
    Category
    Drug
    Distribution
    Distributed nationwide