Drugs & medicalClass I

Mohamed Hagar recalls Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0

Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).

Read the official notice →
Date
2026-03-11
Country
United States
Brand
Mohamed Hagar
Product
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
Classification
Class I
Units
U.S. Nationwide
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2026-03-11
  2. US
    Drugs & medicalClass I

    Abiomed, Inc. recalls Impella RP Flex with SmartAssist. Product Code: 1000323.

    Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.

    FDA · DeviceAbiomed, Inc.Worldwide distribution - US Nationwide and the countries of Austria, Canada,…Official notice →
  3. US
    Drugs & medicalClass II

    MYLAN PHARMACEUTICALS INC recalls Amnesteem (Isotretinoin) Capsules, USP 40 mg, packaged in 3 x 10-Count Prescription Packs, Rx Only, Manufactured for: Mylan…

    Failed Dissolution Specifications

    FDA · DrugMYLAN PHARMACEUTICALS INCNationwide within the United StatesOfficial notice →
  4. US
    Drugs & medicalClass I

    StuffbyNainax recalls MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7

    Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil

    FDA · DrugStuffbyNainaxProduct was distributed to 4 customers in the US.Official notice →
  5. US
  6. US
    Drugs & medicalClass II

    Radnostix recalls Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC 69208-003-15; Order 49317, 49323, 49325, 49329, 49333,…

    Presence of Particulate Matter: Due to production issues

    FDA · DrugRadnostixNationwide in the USA and Puerto RicoOfficial notice →
  7. US
    Drugs & medicalClass I

    ANTHONY TRINH, 123Herbals LLC recalls SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

    Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.

    FDA · DrugANTHONY TRINH, 123Herbals LLCUSA nationwideOfficial notice →
See all drugs & medical recalls →