Recall Atlas
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

Read the official notice →
Date
2026-11-04
Country
United States
Brand
Ritedose
Product
Formoterol Fumarate Inhalation Solution, 20mcg/2mL, packaged in cartons of 30 individually wrapped vials (NDC 76204-030-01) and 60…
Classification
Class II
Units
Nationwide within the U.S
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ritedose recalls

  1. 2023-08-09
  2. Drugs & medicalClass II

    The Ritedose Corporation recalls Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation…

    CGMP deviation: product released prior to supplier approval.

    FDA · DrugThe Ritedose CorporationNationwide in the USOfficial notice →
  3. 2022-04-13
  4. Drugs & medicalClass III

    The Ritedose Corporation recalls 23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx Only, RITEDOSE, 503B Outsourcing Facility, A…

    Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.

    FDA · DrugThe Ritedose CorporationNationwide in the USAOfficial notice →
All 3 Ritedose recalls →

Other drugs & medical recalls in the United States

  1. 2026-11-04
  2. 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 →
  3. 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 →
  4. Drugs & medicalNot Yet Classified

    Trifluent Pharma LLC recalls Tridacaine III / Lidocaine Patch 5%, 15 envelopes containing 1 patch each per pouch, Rx only, Distributed by: Trifluent Pharma San…

    Labeling: Incorrect or Missing Lot and/or Exp Date. Incorrect expiration date printed on the label.

    FDA · DrugTrifluent Pharma LLCUSOfficial notice →
  5. 2026-10-28
  6. Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30.

    A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.

    FDA · DeviceAVID Medical, Inc.US Nationwide distributor in the state of Arizona.Official notice →
  7. Drugs & medicalClass II

    Medline Industries, LP recalls MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit…

    Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

    FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.Official notice →
See all drugs & medical recalls →