Recall Atlas
Drugs & medicalClass I

Amazon.com, Inc. recalls Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO ,…

Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.

Read the official notice →
Date
2022-07-27
Country
United States
Brand
Amazon.com, Inc.
Product
Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO ,…
Classification
Class I
Units
Nationwide within the U.S.A.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-07-27
  2. US
    Drugs & medicalClass II

    Stryker Neurovascular recalls Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413;…

    Microcatheter product label on the carton is missing the microcatheter product drawing/illustration.

    FDA · DeviceStryker NeurovascularWorldwide distribution - US Nationwide distribution in the states of CA, OR,…Official notice →
  3. US
    Drugs & medicalClass II

    Loud Muscle Science recalls Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.

    Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

    FDA · DrugLoud Muscle ScienceThe product was distributed nationwide in the USA and Canada.Official notice →
  4. US
    Drugs & medicalClass I

    Loud Muscle Science recalls Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.

    Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

    FDA · DrugLoud Muscle ScienceThe product was distributed nationwide in the USA and Canada.Official notice →
  5. US
    Drugs & medicalClass II

    Apotex Corp. recalls Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count bottle (NDC…

    Failed dissolution specifications: OOS for dissolution at the 12-month stability time point.

    FDA · DrugApotex Corp.USA NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    CIPLA recalls Difluprednate Ophthalmic Emulsion, 0.05%, 5ml bottles, Rx only, Mfd. by: Cipla Ltd., India At M/S Indoco Remedies Limited., L-32, 33, 34,…

    Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.

    FDA · DrugCIPLANationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass III

    Glenmark Pharmaceuticals Inc., USA recalls Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark…

    Failed Tablet/Capsule Specification : Capsule breakage

    FDA · DrugGlenmark Pharmaceuticals Inc., USAUSA NationwideOfficial notice →
See all drugs & medical recalls →