Drugs & medicalClass I

Boulla LLC recalls ZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. Sacramento, CA 95816, www.zapmax.com

Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.

Read the official notice →
Date
2024-12-11
Country
United States
Brand
Boulla LLC
Product
ZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. Sacramento, CA 95816, www.zapmax.com
Classification
Class I
Units
Nationwide within the United States
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2024-12-11
  2. US
    Drugs & medicalClass II

    Amerisource Health Services LLC recalls Duloxetine Delayed-Release Capsules, USP, 60 mg, Rx only, 1,000 count bottle, Manufactured by: Aurobindo Pharma Limited,…

    CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit

    FDA · DrugAmerisource Health Services LLCPA, OH, PROfficial notice →
  3. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Diltiazem Hydrochloride Extended-Release Capsules, USP 90mg, Twice-a-Day Dosage, Rx Only, 100 Capsules per bottle, Mfd for:…

    cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

    FDA · DrugGlenmark Pharmaceuticals Inc., USANationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    Midlab Incorporated recalls ROYALAB Germ Away Antibacterial Hand Soap, Chloroxylenol 0.1%, NET CONTENTS: ONE U.S. GALLON (3.78 L), Royal Papers, 2701 Hereford St.,…

    cGMP Deviations: Out of specification results for micro in hand soap products.

    FDA · DrugMidlab IncorporatedNationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    American Regent, Inc. recalls Venofer (iron sucrose) Injection, USP 100 mg Elemental Iron per 5 mL (20 mg/mL), 5 mL Single-Dose Vials, Rx Only, For Intravenous Use…

    Presence of Particulate Matter: Potential for glass delamination from the vials.

    FDA · DrugAmerican Regent, Inc.Nationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass II

    Aurobindo Pharma USA Inc recalls Cinacalcet Tablets, 60mg, packaged in: a) 30-count HDPE bottle (NDC 65862-832-30), b) 500-count HDPE bottle (NDC 65862-832-05), Rx Only,…

    cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

    FDA · DrugAurobindo Pharma USA IncUSA NationwideOfficial notice →
  7. US
See all drugs & medical recalls →