Recall Atlas
Drugs & medicalClass II

MACLEODS PHARMA USA, INC recalls Olmesartan Medoxomil, Amlodipine, and Hydrochlorothiazide Tablets 40 mg/10 mg/12.5mg, packaged as a) 30-count bottle, NDC 33342-246-07;…

Failed Dissolution Specifications.

Read the official notice →
Date
2026-11-04
Country
United States
Brand
Macleods Pharma
Product
Olmesartan Medoxomil, Amlodipine, and Hydrochlorothiazide Tablets 40 mg/10 mg/12.5mg, packaged as a) 30-count bottle, NDC 33342-246-07; b)…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Macleods Pharma recalls

  1. 2026-04-01
  2. 2024-05-22
  3. Drugs & medicalClass II

    MACLEODS PHARMA USA, INC recalls Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma…

    Presence of foreign substance: plastic-like substance.

    FDA · DrugMACLEODS PHARMA USA, INCUSA NationwideOfficial notice →
  4. 2023-01-25
  5. Drugs & medicalClass III

    MACLEODS PHARMA USA, INC recalls Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540;…

    Mismatching of the embossing on the tablets (T7) with the embossing mentioned in the package insert (ML63) in the distributed bottles.

    FDA · DrugMACLEODS PHARMA USA, INCNationwide within United States and Puerto Rico.Official notice →
  6. 2022-07-13
  7. Drugs & medicalClass II

    Macleods Pharma Usa Inc recalls Eszopiclone Tablets, USP 1 mg, packaged in 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536,…

    Shortfill: customer complaints of one to three tablets were reported missing from 30 count bottles.

    FDA · DrugMacleods Pharma Usa IncDistributed Nationwide and Puerto Rico.Official notice →
  8. 2022-07-06
  9. Drugs & medicalClass II

    Macleods Pharma Usa Inc recalls Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC #…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    FDA · DrugMacleods Pharma Usa IncProduct was distributed nationwide.Official notice →
  10. 2022-05-11
  11. Drugs & medicalClass II

    Macleods Pharma Usa Inc recalls Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottles (NDC # 33342-045-07), b) 90-count bottles (NDC # 33342-045-10), c) 1000-count…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    FDA · DrugMacleods Pharma Usa IncProduct was distributed nationwide.Official notice →
All 11 Macleods Pharma recalls →

Other drugs & medical recalls in the United States

  1. 2026-11-04
  2. Drugs & medicalClass III

    Prodose, Inc. recalls ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg, 40-caplets per bottle, Distributed by:Prodose, Inc. Ronkonkoma, NY 11779, Made…

    Incorrect label placed on product: Outer carton label correctly identifies drug product in bottle as ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg,but inner label on bottle says ValuHealth Extra Strength…

    FDA · DrugProdose, Inc.Nationwide in the USAOfficial notice →
  3. Drugs & medicalClass II

    Huons Co., Ltd. recalls Carboxymethylcellulose Sodium, 0.5% Lubricant Eye Drops, Sterile, 30 Single-Use Containers, 0.02 FL OZ (0.5 mL) each, Manufactured by:…

    Failed Impurities/Degradation Specification; detection of polyethylene (PE)-related oligomers

    FDA · DrugHuons Co., Ltd.Nationwide within U.S.Official notice →
  4. Drugs & medicalClass II

    Safecor Health, LLC recalls Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC:…

    Manufacturer is recalling batches due to co-mingled tablet.

    FDA · DrugSafecor Health, LLCUS NationwideOfficial notice →
  5. Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Abiraterone Acetate Tablets USP 500 mg, 60-count bottles, Rx only, Distributed by: Glenmark Pharmaceuticals USA, Elmwood…

    Labeling: Not Elsewhere Classified

    FDA · DrugGlenmark Pharmaceuticals Inc., USANationwide within the United StatesOfficial notice →
  6. Drugs & medicalClass II

    The Ritedose Corporation recalls Formoterol Fumarate Inhalation Solution, 20mcg/2mL, packaged in cartons of 30 individually wrapped vials (NDC 76204-030-01) and 60…

    Failed Impurities/Degradation Specification

    FDA · DrugThe Ritedose CorporationNationwide within the U.SOfficial notice →
See all drugs & medical recalls →