Drugs & medicalClass II

Seaway Pharma Inc. recalls Quality Choice No Drip Extra Moisturizing Nasal Pump Mist Oxymetazoline hydrochloride 0.05%, 12 Hour Nasal Decongestant, 1 fl oz (30 mL)…

CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.

Read the official notice →
Date
2024-01-10
Country
United States
Brand
Seaway Pharma Inc.
Product
Quality Choice No Drip Extra Moisturizing Nasal Pump Mist Oxymetazoline hydrochloride 0.05%, 12 Hour Nasal Decongestant, 1 fl oz (30 mL)…
Classification
Class II
Units
MI, PA
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-01-10
  2. US
    Drugs & medicalClass I

    Busse Hospital Disposables, Inc. recalls Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / STERILE - LATEX FREE

    Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance level (SAL) of 10^-6 cannot be…

    FDA · DeviceBusse Hospital Disposables, Inc.US Nationwide distribution.Official notice →
  3. US
    Drugs & medicalClass I

    Insulet Corporation recalls Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.2.3 (current). US: PT-000599- Omnipod 5 App Software Package…

    The bolus calculator is not recording the decimal point if it is the first value entered when changing a bolus dose. This may lead to an over-delivery of insulin to the user if the user does not recognize the error on…

    FDA · DeviceInsulet CorporationWorldwide distribution - US Nationwide and the countries of Germany and UK.Official notice →
  4. US
    Drugs & medicalClass II

    Fresenius Medical Care Holdings, Inc. recalls DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose, packaged in 6000mL bags, Rx only, Fresenius…

    Lack of Sterility Assurance

    FDA · DrugFresenius Medical Care Holdings, Inc.Nationwide within the United StatesOfficial notice →
  5. US
    Drugs & medicalClass III

    Azurity Pharmaceuticals, Inc. recalls Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: Azurity Pharmaceuticals, Woburn, MA…

    Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.

    FDA · DrugAzurity Pharmaceuticals, Inc.USA nationwide.Official notice →
  6. 2024-01-03
  7. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal CARDIAC CATH SET-UP KIT PGYBK, REF 89-10572

    Kit were manufactured and distributed with Edwards Life Sciences TruWave Disposable pressure transducers which were subsequently recalled by Edwards Life Sciences.

    FDA · DeviceDeRoyal Industries IncUS: VirginiaOfficial notice →
  8. US
    Drugs & medicalClass II

    Atrium Medical Corporation recalls Atrium Oasis Drain Single W / AC, Part No. 3600-100

    A sterilization nonconformance prematurely aged the product by 48.3 days, resulting in the expiration date on the label not being accurate. This nonconforming product was inadvertently distributed to customers.…

    FDA · DeviceAtrium Medical CorporationDomestic distribution nationwide. No foreign distribution.Official notice →
See all drugs & medical recalls →