Drugs & medicalClass II

Golden State Medical Supply Inc. recalls PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bottle NDC 60429-734-90;…

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Read the official notice →
Date
2023-12-06
Country
United States
Brand
Golden State Medical Supply
Product
PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bottle NDC 60429-734-90; c)1000-count…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Golden State Medical Supply recalls

  1. 2024-07-03
  2. US
    Drugs & medicalClass II

    Golden State Medical Supply Inc. recalls Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, a) 30 capsules bottles, NDC 60429-165-30; b) 90 capsules bottles, NDC…

    CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit.

    FDA · DrugGolden State Medical Supply Inc.Nationwide in the U.S.Official notice →
  3. 2024-03-06
  4. US
    Drugs & medicalClass II

    Golden State Medical Supply Inc. recalls Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by: Apotek…

    CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex

    FDA · DrugGolden State Medical Supply Inc.Nationwide in the USAOfficial notice →
  5. 2024-02-07
  6. US
  7. 2023-06-14
  8. US
    Drugs & medicalClass II

    Golden State Medical Supply Inc. recalls Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by Apotex Inc., Manufactured by:…

    Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container.

    FDA · DrugGolden State Medical Supply Inc.Nationwide in the USAOfficial notice →
  9. 2022-11-02
  10. US
    Drugs & medicalClass I

    Golden State Medical Supply Inc. recalls Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated,…

    Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets

    FDA · DrugGolden State Medical Supply Inc.USA NationwideOfficial notice →
  11. 2022-10-26
  12. US
    Drugs & medicalClass II

    Golden State Medical Supply Inc. recalls Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS,…

    Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).

    FDA · DrugGolden State Medical Supply Inc.USA nationwideOfficial notice →
All 18 Golden State Medical Supply recalls →

Other drugs & medical recalls in the United States

  1. 2023-12-06
  2. US
    Drugs & medicalClass II

    Becton Dickinson Infusion Therapy Systems Inc. recalls BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

    Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and…

    FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.US Nationwide distribution in the states of CA, NC, MI, WA, CO, FL, NJ, NM,…Official notice →
  3. US
    Drugs & medicalClass I

    Botanical Be recalls Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol…

    Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

    FDA · DrugBotanical BeUSA NationwideOfficial notice →
  4. US
    Drugs & medicalClass I

    Bayer Healthcare Pharmaceuticals Inc. recalls VITRAKVI (larotractenib) oral solution, 20mg/mL, 100 mL bottle, Rx only, Manufactured for Bayer HealthCare Pharmaceuticals…

    Microbial Contamination of Non-Sterile Products: microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing

    FDA · DrugBayer Healthcare Pharmaceuticals Inc.Product was distributed to specialty pharmacies and distributors nationwide…Official notice →
  5. US
  6. US
    Drugs & medicalClass III

    VistaPharm LLC recalls Aminocaproic Acid Oral Solution, 0.25 grams/mL, Rx only, packaged in 8 Fl. Oz. (236.5 mL) HDPE bottles, Manufactured for: VistaPharm,…

    Failed Excipient Specifications: high content of ethylene glycol (EG)

    FDA · DrugVistaPharm LLCNationwide USAOfficial notice →
  7. US
    Drugs & medicalClass III

    Fagron Compounding Services recalls Tropicamide 1% (10mg/mL), Cyclopentolate 1% (10mg/mL), Phenylephrine 2.5% (25mg/mL), Ketorolac 0.5% (5mg/mL), 5 mL bottles, For…

    Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the container is a 0.5mL single-use syringe instead of a 5 mL dropper

    FDA · DrugFagron Compounding ServicesNationwide in the USAOfficial notice →
See all drugs & medical recalls →