Drugs & medicalClass II

Padagis US LLC recalls Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed By Perrigo, Allegan, MI…

CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.

Read the official notice →
Date
2022-09-07
Country
United States
Brand
Padagis
Product
Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed By Perrigo, Allegan, MI…
Classification
Class II
Units
Nationwide in the USA
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Padagis recalls

  1. 2025-03-05
  2. US
    Drugs & medicalClass II

    Padagis US LLC recalls Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only, For Topical Use Only, Manufactured by Padagis, Yeruham, Israel, NDC:…

    Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.

    FDA · DrugPadagis US LLCNationwide in the USAOfficial notice →
  3. 2024-11-27
  4. US
    Drugs & medicalClass III

    Padagis US LLC recalls Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only, Manufactured By Padagis, Minneapolis, MN 55427. NDC: 45802-0063-05

    Subpotent and Superpotent Drug. Out of specification assay results recorded as part of Uniformity of Container test during long-term stability testing.

    FDA · DrugPadagis US LLCNationwide in the USAOfficial notice →
  5. 2023-12-13
  6. US
    Drugs & medicalClass II

    Padagis US LLC recalls Trospium Chloride Extended-Release Capsules, 60 mg, 30 Capsules per bottle, Rx Only, Manufactured By: Sidmak Laboratories (India) Pvt.…

    Failed Tablets/Capsules specifications; missing/broken/extra tablets within the capsules

    FDA · DrugPadagis US LLCNationwide in the USAOfficial notice →
  7. 2023-11-08
  8. US
    Drugs & medicalClass II

    Padagis US LLC recalls Gynazole-1, (Butoconazole Nitrate) Vaginal Cream USP, 2%, Net Wt 5.8 g per pre-filled applicator, packaged in 1 prefilled applicator per…

    Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to manufacture the product rather than Hydrophobic Colloidal Silica as required by the manufacturing process.

    FDA · DrugPadagis US LLCNationwide within the United StatesOfficial notice →
  9. 2023-03-22
  10. US
    Drugs & medicalClass III

    Padagis US LLC recalls Evamist (estradiol transdermal spray), 1.53 mg of estradiol per spray, 0.27 fl oz (8.1 mL) per metered-dose pump, Rx Only, Manufactured by…

    Failed Content Uniformity Specifications: The Spray Content Uniformity (SCU) requirement for Standard Deviation did not meet the requirement at the 18-month stability time point.

    FDA · DrugPadagis US LLCNationwide in the USAOfficial notice →
  11. 2022-01-19
  12. US
All 8 Padagis recalls →

Other drugs & medical recalls in the United States

  1. 2022-09-07
  2. US
    Drugs & medicalClass II

    Aesculap Implant Systems LLC recalls Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar,…

    Potential for the incorrect screw to be included in the package.

    FDA · DeviceAesculap Implant Systems LLCGA, TXOfficial notice →
  3. US
    Drugs & medicalClass II

    Philips North America Llc recalls DigitalDiagnost C50 1.1

    Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, operators will see an incorrect orientation of the image on the first examination due to an issue in…

    FDA · DevicePhilips North America LlcNationwide Distribution including Puerto RicoOfficial notice →
  4. US
    Drugs & medicalClass I

    Medtronic Xomed, Inc. recalls NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306

    The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

    FDA · DeviceMedtronic Xomed, Inc.Worldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice →
  5. US
    Drugs & medicalClass II

    Tsm Brands LLC recalls Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1 PT) 473 ML, Distributed by: TSM Brands LLC, 540 Equinox Ln, Manalapan, NJ 07726, UPC…

    Labeling: Product Contains Undeclared API - product contains undeclared ethyl alcohol

    FDA · DrugTsm Brands LLCDistributed in VA, USAOfficial notice →
  6. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA Inc recalls Neomycin Sulfate Tablets, USP 500 mg , 100-count bottles, Rx only, Distributed by: TEVA PHARMACEUTICALS USA, INC North Wales, PA…

    CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.

    FDA · DrugTeva Pharmaceuticals USA IncNationwide within the United StatesOfficial notice →
  7. US
    Drugs & medicalClass III

    LNK International, Inc. recalls Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS…

    Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.

    FDA · DrugLNK International, Inc.Product was distributed to one retailer who may have further distributed the…Official notice →
See all drugs & medical recalls →